Inhibitors of matrix metallaproteinases

ABSTRACT

The invention provides compounds that inhibit MMPs; methods for treating or preventing cancer, angiogenesis, arthritis, connective tissue disease, cardiovascular disease, inflammation or autoimmune disease in a mammal; a method for inhibiting a matrix metalloproteinase in vivo or in vitro; and a method for imaging a tumor in vivo or in vitro.

RELATED APPLICATION

[0001] The present application claims priority under 35 U.S.C. 119 toU.S. Provisional Application Ser. No. 60/207,874; filed May 30, 2000 andU.S. Provisional Application Ser. No. 60/226,858; filed August 22, 2000;which applications are incorporated herein by reference.

BACKGROUND OF THE INVENTION

[0002] Specific interactions of cells within the extracellular matrixare critical for the normal function of organisms. Alterations of theextracellular matrix are carried out by a family of zinc-dependentendopeptidases called matrix metalloproteinases (MMPs). The alterationsare carried out in various cellular processes such as organ development,ovulation, fetus implantation in the uterus, embyiogenesis, woundhealing, and angiogenesis. Massova, I.; Kotra, L. P.; Fridman, R.;Mobashery, S. FASEB J 1998, 12, 1075; Forget, M. -A.; Desrosier, R. R.;Béliveau, R. Can. J Physiol. Pharmacol. 1999, 77, 465-480.

[0003] MMPs consist of five major groups of enzymes: gelatinases,collagenases, stromelysins, membrane-type MMPs, and matrilysins. Theactivities of MMPs in normal tissue functions is strictly regulated by aseries of complicated zymogen activation processes and inhibition byprotein tissue inhibitors for matrix metalloproteinases (“TIMPs”).Forget, M. -A.; Desrosier, R. R.; Béliveau, R. Can. J. Physiol.Pharmacol. 1999, 77, 465-480; Brew, K.; Dinakarpandian, D.; Nagase, H.Biochim. Biophys. Acta 2000, 1477, 267-283. Westermarck, J.; Kahari, V.M. FASEB J. 1999, 13, 781-792. Excessive MMP activity, when theregulation process fails, has been implicated in cancer growth, tumormetastasis, angiogenesis in tumors, arthritis and connective tissuediseases, cardiovascular disease, inflammation and autoimmune diseases.Massova, I.; Kotra, L. P.; Fridman, R.; Mobashery, S. FASEB J. 1998, 12,1075; Forget, M. -A.; Desrosier, R. R.; Béliveau, R. Can. J Physiol.Pharmocol. 1999, 77, 465-480; Nelson, A. R.; Fingleton, B.; Rothenberg,M. L.; Matrisian, L. M. J. Clin. Oncol. 2000, 18, 1135.

[0004] Increased levels of activity for the human gelatinases MMP-2 andMMP-9 have been implicated in the process of tumor metastasis. Dalberg,K.; Eriksson, E.; Enberg, U.; Kjellman, M.; Backdahl, M. World J. Surg.2000, 24, 334-340. Salo, T.; Liotta, L. A.; Tryggvason, K. J BioL Chem.1983, 258, 3058-3063. Pyke, C.; Ralfkiaer, E.; Huhtala, P.; Hurskainen,T.; Dano, K.; Tryggvason, K. Cancer Res. 1992, 52, 1336-1341. Dumas, V.;Kanitakis, J.; Charvat, S.; Euvrard, S.; Faure, M.; Claudy, A.Anticancer Res. 1999, 19, 2929-2938. As a result, select inhibitors ofMMPs (e.g., MMP-2 and MMP-9) are highly sought.

[0005] Several competitive inhibitors of MMPs are currently known. Theseinhibitors of MMPs take advantage of chelation to the active site zincfor inhibition of activity. Because of this general property, thesecompetitive inhibitors for MMPs are often toxic to the host, which hasbeen a major impediment in their clinical use. Greenwald, R. A. Ann. N.Y Acad. Sci. 1999, 878, 413-419; (a) Michaelides, M. R.; Curtin, M. L.Curr. Pharm. Des. 1999, 5, 787-819. (b) Beckett, R. P.; Davidson, A. H.;Drummond, A. H.; Huxley, P.; Whittaker, M. Drug Disc. Today 1996, 1,16-26.

[0006] Gelatinases have been shown to function in both female ovulationand inplantation of zygotes in the womb. The female contains a pair ofgonads, a system of ducts and chambers to conduct the gametes as well asto house the embryo and fetus, and external genitalia that facilitatereproductive function. The female gonads, the ovaries, lie in theabdominal cavity below most of the digestive system. Each ovary isenclosed in a tough protective capsule and contains many follicles. Afollicle consists of one egg cell surrounded by one or more layers offollicle cells, which nourish and protect the developing egg cell. Allof the 400,000 follicles a woman will ever have are formed at birth. Ofthese, only several hundred will be released during the woman'sreproductive years. After puberty, one (or rarely two or more) folliclematures and releases its egg during each menstrual cycle. The cells ofthe follicle also produce the primary female sex hormones, the estrogen.When ovulation occurs, the egg is expelled from the follicle (much likea small volcano), and the remaining follicular tissue grows within theovary to form a solid mass called the corpus luteum. The corpus luteumsecretes progesterone, the hormone of pregnancy, and additionalestrogen. If the egg is not fertilized, the corpus luteum degeneratesand a new follicle matures during the next cycle.

[0007] The female reproductive system is not completely closed, and theegg cell is expelled into the abdominal cavity near the opening of theoviduct, or fallopian tube. The oviduct has a funnellike opening, andcilia on the inner epithelium lining the duct help collect the egg cellby drawing fluid from the body cavity into the duct. The cilia alsoconvey the egg cell down the duct to the uterus, commonly called thewomb. The uterus is a thick, muscular organ shaped much like anupside-down pear. It is remarkably small; the uterus of a woman who hasnever been pregnant is about 7 cm long and 4-5 cm wide at its widestpoint. The unique arrangement of muscles that make up the bulk of theuterine wall allow it to expand to accommodate a 4-kg fetus. The innerlining of the uterus, the endometrium, is richly supplied with bloodvessels.

[0008] The pattern of hormone secretion controlling female reproductiondiffers strikingly from the male pattern, reflecting a cyclic nature offemale reproduction.

[0009] Two different types of cycles occur in female mammals. Humans andmany other primates have menstrual cycles, whereas other mammals haveestrous cycles. In both cases, ovulation occurs at a time in the cycleafter the endometrium has started to thicken and become more extensivelyvascularized, which prepares the uterus for the possible implantation ofan embryo.

[0010] The menstrual cycle averages 28 days, but only about 30% of womenhave cycle lengths within a day or two of the statistical 28 days.Cycles vary from one woman to another, ranging from about 20 to 40 days.In some women the cycles are usually very regular, but in otherindividuals the timing varies from cycle to cycle.

[0011] Paralleling the menstrual cycle is an ovarian cycle. It beginswith the follicular phase, during which several follicles in the ovarybegin to grow. The egg cell enlarges and the coat of follicle cellsbecomes multi-layered. Of the several follicles that start to grow, onlyone usually continues to enlarge and mature, while the othersdegenerate. The maturing follicle develops an internal fluid-filledcavity and grows very large, forming a bulge near the surface of theovary. The follicular phase ends with ovulation when the follicle andadjacent wall of the ovary rupture, releasing the egg cell. Thefollicular tissue that remains in the ovary after ovulation istransformed into the corpus luteum, an endocrine tissue that secretesfemale hormones during what is called the luteal phase of the ovariancycle. The next cycle begins with a new growth of follicles.

[0012] Contraception literally means “against taking,” in this case, thetaking in of a child. The term has come to mean preventing a pregnancythrough one of several methods. These methods fall into three maincategories: (1) preventing the egg and sperm from meeting in the femalereproductive tract, (2) preventing implantation of a zygote, and (3)preventing the release of mature eggs and sperm from the gonads.

[0013] Besides complete abstinence, the methods that prevent release ofgametes are the most effective means of birth control. Chemicalcontraception (birth control pills) have failure rates of less than 1%,and sterilization is nearly 100% effective. Birth control pills arecombinations of a synthetic estrogen and a synthetic progestin(progesterone-like hormone). These two hormones act by negative feedbackto stop the release of GnRH by the hypothalamus and FSH (an estrogeneffect) and LH (a progestin effect) by the pituitary. By blocking LHrelease, the progestin prevents ovulation. As a backup measure, theestrogen inhibits FSH secretion so no follicles develop. Chemicalcontraception has been the center of much debate, particularly becauseof the long-term side effects of the estrogens. No solid evidence existsfor cancers caused by the pill, but cardiovascular problems are a majorconcern. Birth control pills have been implicated in blood clotting,atherosclerosis, and heart attacks. Smoking while using chemicalcontraception increases the risk of mortality tenfold or more. Campbell,N.; Biology, 2nd Ed., Benjamin/Cummings Publ., Redwood City, La., 1990.

[0014] Accordingly, there is a current need for inhibitors of MMPs. Suchinhibitors would be useful to treat or prevent cancer, tumor metastasis,angiogenesis in tumors, contraception, arthritis and connective tissuediseases, cardiovascular disease, inflammation or autoimmune diseases.Preferred inhibitors may exhibit selectivity for one or more specificMMPs than known competitive inhibitors. In addition, additional methodsthat prevent the release of gametes are needed. Suth methods willpreferably not include negative long-term side-effects.

SUMMARY OF THE INVENTION

[0015] The present invention provides compounds that inhibit MMPs.Accordingly, there is provided a compound of the invention which is acompound of formula (I):

[0016] wherein

[0017] A—X—M is a hydrophobic group;

[0018] D is O, S, (C₁-C₆)alkyl, a direct bond, SO₂, SO, C(═O)NR, C(═O)O,NRC(═O), or OC(═O);

[0019] E is a direct bond, (C₁-C₆)alkyl, (C₃-C₈)cycloalkyl,(C₂-C₆)alkenyl, or (C₂-C₆)alkynyl, wherein any alkyl, cycloalkyl,alkenyl, or alkynyl of E is optionally substituted with one or more(C₁-C₆)alkyl, hydroxy, (C₁-C₆)alkoxy, cyano, nitro, halo, SR, NRR, orCOOR, wherein each R is independently H or (C₁-C₆)alkyl;

[0020] J is S or O;

[0021] G, T, and Q are each independently H, (C₁-C₆)alkyl, or cyano;

[0022] or a pharmaceutically acceptable salt thereof.

[0023] The present invention also provides a pharmaceutical compositionthat comprises a compound of formula (I) and a pharmaceuticallyacceptable carrier.

[0024] The present invention also provides a radiolabeled compoundcomprising a compound of formula (I) and a radionuclide.

[0025] The present invention also provides a pharmaceutical compositionthat comprises a radiolabeled compound of formula (J) and apharmaceutically acceptable carrier.

[0026] The present invention also provides a therapeutic method forpreventing or treating a pathological condition or symptom in a mammal,such as a human, wherein the activity of an MMP is implicated andinhibition of its action is desired, comprising administering to amammal in need of such therapy, an effective amount of a compound offormula (I), or a pharmaceutically acceptable salt thereof.

[0027] The present invention also provides a method for treating orpreventing cancer, angiogenesis, arthritis, connective tissue disease,cardiovascular disease, inflammation or autoimmune disease in a mammalinflicted with or at risk thereof comprising administering to the mammalin need of such treatment or prevention an effective amount of acompound of formula (I).

[0028] The present invention also provides a method for treating orpreventing cancer in a mammal inflicted with or at risk thereofcomprising administering to the mammal in need of such therapy aneffective amount of a compound of formula (I), or a pharmaceuticallyacceptable salt thereof in conjunction with a chemotherapeutic agent, ora pharmaceutically acceptable salt thereof.

[0029] The present invention also provides a method for inhibiting amatrix metalloproteinase comprising a zinc atom, the method comprisingcontacting the matrix metalloproteinase with a compound with a groupthat can be activated for nucleophilic substitution by the zinc atom andcan form a covalent bond with a nucleophile of the matrixmetalloproteinase.

[0030] The present invention also provides a method for inhibiting agelatinase comprising a zinc atom, the method comprising contacting thegelatinase with a compound with a group that can be activated fornucleophilic substitution by the zinc atom and can form a covalent bondwith a nucleophilic site of the gelatinase.

[0031] The present invention also provides a method for imaging a tumorin a mammal inflicted with a tumor comprising administering to themammal an effective amount of a radiolabeled compound of formula (I), ora pharmaceutically acceptable salt thereof, and detecting the presenceof the radiolabeled compound.

[0032] The present invention also provides a method to image MMPactivity in a tumor and/or a vasculature comprising contacting theorganism (e.g., in vivo) with an effective amount of a compound thepresent invention, wherein the compound of formula (I) comprises aradionuclide; or a pharmaceutically acceptable salt thereof.

[0033] The present invention also provides a method for imaging MMPactivity in a tumor in a mammal inflicted with a tumor comprisingadministering to the mammal in need of such imaging an effective amountof a compound the present invention, wherein the compound of formula (I)comprises a radionuclide; or a pharmaceutically acceptable salt thereof.

[0034] The present invention also provides a method for preventingovulation in a mammal (e.g., human) at risk thereof comprisingadministering to the mammal an effective amount of a compound of formula(I).

[0035] The present invention also provides a method for preventing theimplantation of a fertilized egg into the uterus of a mammal (e.g.,human) in need thereof comprising administering to the mammal aneffective amount of a compound of formula (I).

BRIEF DESCRIPTION OF THE FIGURES

[0036]FIG. 1 illustrates a mechanism-based inhibition of an MMP by acompound of the present invention.

[0037]FIG. 2 illustrates a synthesis of compounds of the presentinvention.

[0038]FIG. 3 illustrates a mechanism-based inhibition of an MMP by acompound of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

[0039] The following definitions are used, unless otherwise described:halo is fluoro, chloro, bromo, or iodo. Alkyl, alkoxy, alkenyl, alkynyl,etc. denote both straight and branched groups; but reference to anindividual group such as “propyl” embraces only the straight chainvariant, a branched chain isomer such as “isopropyl” being specificallyreferred to. Bicyclic aryl denotes an ortho-fused bicyclic carbocyclicsubstituent having about nine to ten ring atoms in which at least onering is aromatic. Monocyclic heteroaryl encompasses a substituentattached via a ring carbon of a monocyclic aromatic ring containing fiveor six ring atoms consisting of carbon and one to four heteroatoms eachselected from the group consisting of non-peroxide oxygen, sulfur, andN(X) wherein X is absent or is H, O, (C₁-C₄)alkyl, phenyl or benzyl.Bicyclic heteroaryl encompasses a substituent of an ortho-fused bicyclicheterocycle of about eight to ten ring atoms derived therefrom,particularly a benzyl-derivative or one derived by fusing a propylene,trimethylene, or tetramethylene divalent substituent thereto. Bicyclicalkyl encompasses a substituent of an ortho-fused bicyclic alkyl ofabout eight to ten ring atoms containing five or six ring atomsconsisting of carbon and one to four ring atoms consisting ofheteroatoms selected from the group consisting of non-peroxide oxygen,sulfur, and N(X) wherein X is absent or is H, O (C₁-C₄)alkyl, phenyl orbenzyl.

[0040] It will be appreciated by those skilled in the art that compoundsof the invention having a chiral center may exist in and be isolated inoptically active and racemic forms. Some compounds may exhibitpolymorphism. It is to be understood that the present inventionencompasses any racemic, optically-active, polymorphic, orstereoisomeric form, or mixtures thereof, of a compound of theinvention, which possess the useful properties described herein, itbeing well known in the art how to prepare optically active forms (forexample, by resolution of the racemic form by recrystallizationtechniques, by synthesis from optically-active starting materials, bychiral synthesis, or by chromatographic separation using a chiralstationary phase) and how to determine MMP inhibition activity using thestandard tests described hereinbelow, or using other similar tests whichare well known in the art.

[0041] As used herein, “ovulation” is the release of an ovum from theovarian follicle. Stedman's Medical Dictionary, 25th Ed., Illustrated,Williams & Wilkins, Baltimore, 1990, p.1116.

[0042] As used herein, “ovum” is the female sex (reproductive) cell.When fertlized by a spermatozoon, an ovum is capable of developing intoa new individual of the same species. Stedman's Medical Dictionary, 25thEd., Illustrated, Williams & Wilkins, Baltimore, 1990, p.1116.

[0043] As used herein, “fertiliziation” is the process beginning withpenetration of the secondary oocyte by the spermatozoon and completed byinfusion of the male and female pronuclei. Stedman's Medical Dictionarv,25th Ed., Illustrated, Williams & Wilkins, Baltimore, 1990, p.573.

[0044] As used herein, a “uterus” is the womb, metra, or the hollowmuscular organ in which the impregnated ovum is developed into thechild. Stedman's Medical Dictionary, 25th Ed., Illustrated, Williams &Wilkins, Baltimore, 1990, pp.1677-1678.

[0045] Specific and preferred values listed below for substituents(i.e., groups) and ranges are for illustration only; they do not excludeother defined values or other values within defined ranges for thesubstituents.

[0046] Specifically, (C₁-C₆)alkyl can be methyl, ethyl, propyl,isopropyl, butyl, iso-butyl, sec-butyl, pentyl, 3-pentyl, or hexyl;(C₁-C₆)alkoxy can be methoxy, ethoxy, propoxy, isopropoxy, butoxy,iso-butoxy, sec-butoxy, pentoxy, 3-pentoxy, or hexyloxy; (C₂-C₆)alkenylcan be vinyl, allyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl,3-butenyl, 1,-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-hexenyl,2-hexenyl, 3-hexenyl, 4-hexenyl, or 5-hexenyl; (C₂-C₆)alkynyl can beethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl,1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-hexynyl, 2-hexynyl,3-hexynyl, 4-hexynyl, or 5-hexynyl; (C₁-C₆)alkanoyl can be acetyl,propanoyl or butanoyl; (C₂-C₆)alkanoyloxy can be acetoxy, propanoyloxy,butanoyloxy, isobutanoyloxy, pentanoyloxy, or hexanoyloxy;(C₃-C₈)cycloalkyl can be cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, cycloheptyl, or cyclooctyl; aryl can be phenyl, indenyl,5,6,7,8-tetrahydronaphthyl, or naphthyl and heteroaryl can be furyl,imidazolyl, tetrazolyl, pyridyl, (or its N-oxide), thienyl, pyrimidinyl(or its N-oxide), indolyl, or quinolyl (or its N-oxide); bicyclic arylcan be indenyl or naphthyl; monocyclic heteroaryl can be furyl,imidazolyl, triazolyl, triazinyl, oxazoyl, isoxazoyl, thiazolyl,isothiazoyl, pyrazolyl, pyrrolyl, pyrazinyl, tetrazolyl, pyridyl (or itsN-oxide), thienyl, or pyrimidinyl (or its N-oxide), bicyclic heteroarylcan be quinolyl (or its N-oxide); and bicyclic alkyl can bedecahydroquinoline or decahydronaphthalene (cis and trans).

[0047] As used herein, an “amino acid” is a natural amino acid residue(e.g. Ala, Arg, Asn, Asp, Cys, Glu, Gln, Gly, His, Hyl, Hyp, Ile, Leu,Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, and Val) in D or L form, as wellas unnatural amino acid (e.g. phosphoserine; phosphothreonine;phosphotyrosine; hydroxyproline; gamma-carboxyglutamate; hippuric acid;octahydroindole-2-carboxylic acid; statine;1,2,3,4,-tetrahydroisoquinoline-3-carboxylic acid; penicillamine;ornithine; citruline; α-methyl-alanine; para-benzoylphenylalanine;phenylglycine; propargylglycine; sarcosine; and tert-butylglycine)residue having one or more open valences. The term also comprisesnatural and unnatural amino acids bearing amino protecting groups (e.g.acetyl, acyl, trifluoroacetyl, or benzyloxycarbonyl), as well as naturaland unnatural amino acids protected at carboxy with protecting groups(e.g. as a (C₁-C₆)alkyl, phenyl or benzyl ester or amide). Othersuitable amino and carboxy protecting groups are known to those skilledin the art (See for example, T. W. Greene, Protecting Groups In OrganicSynthesis; Wiley: New York, 1981; D. Voet, Biochemistry, Wiley: NewYork, 1990; L. Stryer, Biochemistry, (3rd Ed.), W.H. Freeman and Co.:New York, 1975; J. March, Advanced Organic Chemistry Reactions,Mechanisms and Structure, (2nd Ed.), McGraw Hill: New York, 1977; F.Carey and R. Sundberg, Advanced Organic Chemistry, Part B: Reactions andSynthesis, (2nd Ed.), Plenum: New York, 1977; and references citedtherein). According to the invention, the amino or carboxy protectinggroup can also comprise a radionuclide (e.g., Fluorine-18, Iodine-123,or Iodine-124).

[0048] As used herein, an “electrophile” refers to a chemical species,ion, or a portion of a compound which, in the course of a chemicalreaction, will acquire electrons, or share electrons, to form othermolecules or ions. Electrophiles are ordinarily thought of as cationicspecies (positively charged). McGraw-Hill Concise Encyclopedia ofScience & Technology, McGraw-Hill, p.715, 4^(th) Edition, NY, N.Y.(1998).

[0049] As used herein, a “nucleophile” refers to a chemical species,ion, or a portion of a compound which, in the course of a chemicalreaction, will lose electrons, or share electrons, to form othermolecules or ions. Nucleophiles are ordinarily thought of as anionicspecies (negatively charged). Typical nucleoplic species include, e.g.,hydroxyl (OH), halo (F, Cl, Br, or I), cyano (CN), alkoxy (CH₃CH₂O),carboxyl (COO), and thio (S). McGraw-Hill Concise Encyclopedia ofScience & Technology, McGraw-Hill, p.715, 4th Edition, NY, N.Y. (1998).

[0050] As used herein, a “peptide” is a sequence of 2 to 25 amino acids(e.g. as defined hereinabove) or peptidic residues having one or moreopen valences. The sequence may be linear or cyclic. For example, acyclic peptide can be prepared or may result from the formation ofdisulfide bridges between two cysteine residues in a sequence. A peptidecan be linked through the carboxy terminus, the amino terminus, orthrough any other convenient point of attachment, such as, for example,through the sulfur of a cysteine. Peptide derivatives can be prepared asdisclosed in U.S. Pat. Nos. 4,612,302; 4,853,371; and 4,684,620. Peptidesequences specifically recited herein are written with the aminoterminus on the left and the carboxy terminus on the right.

[0051] As used herein, a “hydrophobic group” or “hydrophobic moiety”refers to a group that is relatively non-polar and will have arelatively minimal affinity for water. The nature of the hydrphobicgroup (i.e., A—X—M) is not important, provided the hydrophobic groupfits into the pocket and has a favorable interaction (e.g., binding)with the enzyme. The hydrophobic group, while being relativelyhydrophobic, can include one or more heteroatoms (e.g., S, O, or N) thatcan have an electrostatic charge or can include one or more groups(e.g., esters or amides) that can have an electrostatic charge, providedthe hydrophobic group fits into the pocket and has a favorableinteraction with the enzyme.

[0052] Any suitable hydrophobic group can be employed as A—X—M, providedthe hydrophobic group fits into the pocket and has a favorableinteraction (e.g., binding) with the enzyme. For example, thehydrophobic group can include a straight-chained or branched hydrocarbonchain (e.g., alkyl, alkenyl, or alkynyl), an aryl group (e.g.,monocyclic or bicylic), a heteroaryl group (e.g., monocyclic orbicylic), a cycloalkyl group, an amino acid, a peptide, or a combinationthereof.

[0053] In one embodiment, A—X—M can be a saturated or partiallyunsaturated hydrocarbon chain comprising one or more carbon atoms andoptionally comprising one or more oxy (—O—), thio (—S—), sulfinyl(—SO—), sulfonyl (S(O)₂—), or NR_(f) in the chain, wherein each Rf isindependently hydrogen or (C₁-C₆)alkyl. The saturated or partiallyunsaturated hydrocarbon chain can optionally be substituted with one ormore oxo (═O), hydroxy, cyano, halo, nitro, trifluoromethyl,trifluoromethoxy, (C₁-C₆)alkyl, (C₁-C₆)alkoxy,(C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl, aryl, heteroaryl,(C₃-C₈)cycloalkyl(C₁-C₆)alkyl, (aryl)(C₁-C₈)alkyl,(heteroaryl)(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl oxy, (aryl)oxy,(heteroaryl)oxy, (C₃-C₈)cycloalkyl, (aryl)oxy(aryl),(heteroaryl)oxy(heteroaryl), (C₃-C₈)cycloalkyl oxy (C₁-C₆)alkyl,(aryl)oxy (C₁-C₆)alkyl, or (heteroaryl)oxy (C₁-C₆)alkyl. In addition,any aryl, (C₃-C₈)cycloalkyl, or heteroaryl can optionally be substitutedwith one or more oxo (═O), hydroxy, cyano, halo, nitro, trifluoromethyl,trifluoromethoxy, (C₁-C₆)alkyl, (C₁-C₆)alkoxy,(C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl, aryl, heteroaryl,(C₃-C₈)cycloalkyl(C₁-C₆)alkyl, (aryl)(C₁-C₈)alkyl,(heteroaryl)(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl oxy, (aryl)oxy,(heteroaryl)oxy, (C₃-C₈)cycloalkyl, (aryl)oxy(aryl),(heteroaryl)oxy(heteroaryl), (C₃-C₈)cycloalkyl oxy (C₁-C₆)alkyl,(aryl)oxy (C₁-C₆)alkyl, or (heteroaryl)oxy (C₁-C₆)alkyl.

[0054] When A—X—M is a “partially unsaturated” group, such group maycomprise one or more (e.g. 1 or 2) carbon-carbon double or triple bonds.For example, when A—X—M is a partially unsaturated (C₁-C₆)alkyl, it canbe vinyl, allyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl,3-butenyl, 1,3-butadienyl, 1-pentenyl, 2-pentenyl, 3-pentenyl,4-pentenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 2,4-hexadienyl,5-hexenyl, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl,3-butynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl,5-hexene-1-ynyl, 2-hexynyl, 3-hexynyl, 3-hexen-5-ynyl, 4-hexynyl, or5-hexynyl.

[0055] A specific value for A—X—M is A and M are each independentlyphenyl or monocyclic heteroaryl, wherein any phenyl or heteroaryl isoptionally substituted with one or more (e.g., 1, 2, 3, or 4) hydroxy,(C₁-C₆)alkyl, (C₁-C₆)alkanoyl, (C₁-C₆)alkanoyloxy, (C₁-C₆)alkoxy, cyano,nitro, halo, trifluoromethyl, trifluoromethoxy, SR, NRR, or COOR; and

[0056] X is O S, SO, SO₂, C(═O)NR, C(═O)O, NRC(═O), OC(═O), NR, a directbond, or (C₁-C₆)alkyl optionally substituted with one or more hydroxy,(C₁-C₆)alkoxy, cyano, nitro, halo, SR, NRR, or COOR.

[0057] Another specific value for A—X—M is bicyclic aryl (e.g.,naphthyl), bicyclic heteroaryl, or bicyclic alkyl; wherein any aryl,heteroaryl or alkyl is optionally substituted with one or more (e.g., 1,2, 3, or 4) hydroxy, (C₁-C₆)alkyl, (C₁-C₆)alkanoyl, (C₁-C₆)alkanoyloxy,(C₁-C₆)alkoxy, cyano, nitro, halo, trifluoromethyl, trifluoromethoxy,SR, NRR, or COOR;

[0058] wherein each R is independently H, (C₁-C₆)alkyl, phenyl, benzyl,or phenethyl.

[0059] A specific value for A is phenyl or monocyclic heteroaryl.Another specific value for A is phenyl.

[0060] A specific value for M is phenyl or monocyclic heteroaryl.Another specific value for M is phenyl.

[0061] A specific value for X is O, S, SO, SO₂, C(═O)NR, C(═O)O,NRC(═O), OC(═O), NR, a direct bond, or (C₁-C₆)alkyl. Another specificvalue for X is O.

[0062] Another specific value for A—X—M is:

[0063] wherein

[0064] X′ is O, (C₁-C₆)alkyl (e.g., CH₂), or a direct bond;

[0065] Y′ is N or (C₁-C₆)alkyl (e.g., CH₂); and

[0066] Z′ is halo, (C₁-C₆)alkoxy (e.g., OCH₃), or hydroxy.

[0067] Another specific value for A-X-M is:

[0068] wherein

[0069] each W′ is independently N or CH; and

[0070] Z′ is halo, (C₁-C₆)alkoxy (e.g., OCH₃), or hydroxy.

[0071] Another specific value for A—X—M is:

[0072] wherein

[0073] n′ is about 1 to about 4; and

[0074] Z′ is halo, (C₁-C₆)alkoxy (e.g., OCH₃), or hydroxy.

[0075] Another specific value for A—X—M is:

[0076] wherein

[0077] R′ is O, (C₁-C₆)alkyl (e.g., CH₂), or S; and

[0078] m′ is about 2 to about 7.

[0079] Another specific value for A—X—M is:

[0080] wherein

[0081] n′ is about 1 to about 4.

[0082] Another specific value for A—X—M is:

[0083] wherein

[0084] R′ is O, CH₂, or S.

[0085] A specific value for D is SO₂.

[0086] A specific value for E is (C₁-C₆)alkyl. Another specific valuefor E is methyl.

[0087] A specific value for (C₁-C₆)alkyl is methyl.

[0088] A specific value for J is S.

[0089] A specific value for G is hydrogen.

[0090] A specific value for T is hydrogen.

[0091] A specific value for Q is hydrogen.

[0092] A specific compound of the present invention is a compound offormula (I) wherein A is phenyl, M is phenyl, X is O, D is SO₂, E ismethyl, J is S, G is hydrogen, T is hydrogen, and Q is hydrogen.

[0093]FIG. 2 illustrates a synthesis for compounds 1-4.4-phenoxythiophenol 10 was prepared from the commercially available4-phenoxyphenol 7 via the 3 step procedure illustrated by Newman andKarnes. Newman M. S.; Kames H. A. J. Org. Chem., 1996, 31, 3980-3984.Subsequent alkylation of 10 with allyl bromide, 4-bromo-1-butene and5-bromo-1-pentene respectively, led to the sulfanyl compounds 11-13 ingood yield. Although the epoxidation of 12 and 13 with mCPBA wasrelatively quick, taking only 2-3 days, the formation of 11 took 7 daysand required a large excess of mCPBA. Finally, the conversion of theepoxides 4-6 to their corresponding thiirane derivatives 1-3, wasaccomplished via the treatment of each epoxide with ammoniumthiocyanatein THF/water. Although the thiiranes 2 and 3 were isolated in highyield, 93% and 85% respectively, thiirane 1 could only be recovered in avery poor (i.e., 14%) yield.

[0094] Processes for preparing compounds of formula (I) or for preparingintermediates useful for preparing compounds of formula (I) are providedas further embodiments of the invention. Intermediates useful forpreparing compounds of formula (I) are also provided as furtherembodiments of the invention.

[0095] A compound of formula (I) wherein J is S can be prepared bytreating a corresponding compound of formula (I) wherein J is 0 with asuitable sulfonating reagent. See, e.g., March, Advanced OrganicChemistry, Reactions, Mechanisms and Structure, 2^(nd) Ed., 1977 andCarey & Sundberg, Advanced Organic Chemistry, Part B: Reactions, 2^(nd)Ed., 1983.

[0096] A compound of formula (I) wherein J is O can be prepared byepoxidizing a corresponding compound of formula (I) wherein the ringthat includes J is an alkene. See, e.g., March, Advanced OrganicChemistry, Reactions, Mechanisms and Structure, 2^(nd) Ed., 1977 andCarey & Sundberg, Advanced Organic Chemistry, Part B: Reactions, 2^(nd)Ed., 1983.

[0097] A compound of formula (I) wherein D is SO₂ and J is O can beprepared by oxidizing a corresponding compound of formula (I) wherein Dis S. See, e.g., March, Advanced Organic Chemistry, Reactions,Mechanisms and Structure, 2^(nd) Ed., 1977 and Carey & Sundberg,Advanced Organic Chemistry, Part B: Reactions, 2^(nd) Ed., 1983.

[0098] A specific group of the compounds of the present invention, thatcan be activated by zinc for nucleophilic substitution and that can forma covalent bond with a nucleophile of the matrix metalloproteinase,includes a thiirane ring. Another specific group of the compounds of thepresent invention, that can be activated by zinc for nucleophilicsubstitution and that can form a covalent bond with a nucleophile of thematrix metalloproteinase, includes an oxirane ring. In addition, aspecific nucleophile of the matrix metalloproteinase which can form acovalent bond with the group of the compounds of the present invention(e.g., thiirane or oxirane) is located at the amino acid residuecorresponding to residue 404 of the matrix metalloproteinase, whereinthe numbering is based on the active site general base for gelatinase A,which is observed in other MMPs. More specifically, the nucleophile is acarboxy (i.e., COO⁻) oxygen atom located at amino acid residuecorresponding to residue 404 of the matrix metalloproteinase, whereinthe numbering is based on the active site general base for gelatinase A,which is observed in other MMPs. See, FIG. 1.

[0099] The matrix metalloproteinase can be a human matrixmetalloproteinase. In addition, the matrix metalloproteinase can be agelatinase, collagenase, stromelysin, membrane-type MMP, or matrilysin.Specifically, the gelatinase can be MMP-2 or MMP-9.

[0100] According to the method of the invention, the matrixmetalloproteinase can be contacted with the compound, e.g., a compoundof formula (I), in vitro. Alternatively, the matrix metalloproteinasecan be contacted with the compound, e.g., a compound of formula (I), invivo.

[0101] Without being bound by any particular theory, coordination of athiirane in a compound of formula (I) with the enzyme active-site zincion is believed to activate the thiirane for modification by anucleophile of the enzyme. See, FIG. 1. A computational model based onthree-dimensional homology modeling for this enzyme with compound 1indicates that the biphenyl group would fit in the active siteanalogously to the same group in certain known reversible inhibitors ofMMP-2 and MMP-9, as analyzed by X-ray structure determination. Freskos,J. N.; Mischke B. V.; DeCrescenzo, G. A.; Heintz, R.; Getman, D. P.;Howard, S. C.; Kishore, N. N.; McDonald, J. J.; Munie, G. E.; Rangwala,S.; Swearingen, C. A.; Voliva, C.; Welsch, D. J. Bioorg. & Med. Chem.Letters, 1999, 9, 943-948. Tamura, Y.; Watanabe, F.; Nakatani, T.;Yasui, K.; Fuji, M.; Komurasaki, T.; Tsuzuki, H.; Maekawa, R.; Yoshioka,T.; Kawada, K.; Sugita, K.; Ohtani, M. J. Med. Chem. 1998, 41, 640-649.As such, the biphenyl ether moiety in compounds 1-4 is believed to fitin the P1′ subsite of gelatinases, which is a deep hydrophobic pocket.(a) Morgunova, E.; Tuuttila, A.; Bergmann, U.; Isupov, M.; Lindqvist,Y.; Schneider, G.; Tryggvason, K. Science 1999, 284, 1667-1670. (b)Massova, I.; Fridman, R.; Mobashery, S. J. Mol. Mod. 1997, 3, 17-34;Olson, M. W.; Bernardo, M. M.; Pietila, M.; Gervasi, D. C.; Toth, M.;Kotra, L. P.; Massova, I.; Mobashery, S.; Fridman, R. J. Biol. Chem.,2000, 275, 2661-2668. This binding mode brings the sulfur of thethiirane in 1 into the coordination sphere of the zinc ion. See, FIG. 1.The models also indicated that the thiirane moiety in compounds 2 and 3,with longer carbon backbones, would not be able to coordinate with thezinc ion as well as compound 1, but would fit in an extendedconfiguration in the active site.

[0102] It is believed that the high specificity of certain compounds ofthe invention for a targeted enzyme arises predominantly from threefactors. (i) the compounds satisfy the binding specificity requirementsat the active site. In this respect these compounds are not anydifferent from conventional reversible or affinity inhibitors. (ii)Furthermore, the structural features of the inhibition should allow itto undergo chemical activation by the zinc atom of the enzyme togenerate an electrophilic species within the active site. (iii) Finally,there should be a nucleophilic amino-acid residue in the active site, inthe proper orientation, to react with the electrophilic species (e.g.,thiirane ring), resulting in irreversible enzyme inactivation.

[0103] By selecting a hydrophobic group (e.g., A—X—M) located a specificdistance from a group (e.g., D) that can bind (e.g., hydrogen bond) withone or more sites in the enzyme (e.g., amino acid residue 191 and/oramino acid residue 192, in gelatinase A), which is in turn located aspecific distance from a thiirane ring that can coordinate with theenzyme active-site zinc atom, one can prepare selective mechanism-basedinhibitors for a given MMP. See, FIG. 1.

[0104] Accordingly, preferred MMP inhibitors have a hydrophobic arylmoiety (e.g., A—X—M) that can fit in the deep hydrophobic pocket (i.e.,P₁′ subsite) of an MMP. In addition, preferred mechanism-based MMPinhibitors also have a thiirane ring that can coordinate with the enzymeactive-site zinc ion, and be modified by a nucleophile (e.g.,carboxylate group of amino acid residue 404 of MMP-2) in the enzymeactive site. See, FIG. 1. The preferred MMP inhibitors can optionallyinclude a second group (e.g., D) that can coordinate with one or moresites in the enzyme. Specifically, the second group can optionallyhydrogen bond to the one or two proton donors (e.g., amino acid residuecorresponding to residue 191 and/or amino acid residue corresponding toresidue 192 of MMP-2) in the enzyme active site. See, FIG. 1.

[0105] The present invention provides a method for identifying amechanistic based MMP inhibitor. The method includes providing acompound wherein (1) a hydrophobic moiety of the compound fits into ahydrophobic pocket of the MMP; (2) the compound has one or two groupsthat can hydrogen bond with one or two hydrogen donors of the MMP,wherein the hydrogen donors of the MMP are located at amino acid residuecorresponding to residue 191 and amino acid residue corresponding toresidue 192 of MMP-2; (3) the compound has an electrophilic group thatcan covalently bond with a nucleophile of the MMP, wherein thenucleophile of the MMP is located at amino acid residue corresponding toresidue 404 of MMP-2; and/or (4) the compound includes a group that cancoordinate with the zinc ion of the MMP.

[0106] Preferred MMP inhibitors have a thiirane or oxirane such that thesulfur or oxygen atom of the thiirane or oxirane is located about 3angstroms to about 4 angstroms from the zinc ion. The suitable MMPinhibitors can also include a thiirane or oxirane ring located about 3angstroms to about 5 angstroms from the active site nucleophile. See,FIGS. 1 and 3.

[0107] Radiolabeled compounds of formula (I) are also useful as imagingagents for imaging cells comprising MMP's. Accordingly, the inventionalso provides compounds of formula (I) that include one or moredetectable radionuclides (e.g., one or more metallic radionuclide and/orone or more non-metallic radionuclides). For example, a detectableradionuclide can be incorporated into a compound by replacing an atom ofthe compound of formula (I) with a radionuclide (e.g., non-metallicradionuclide). Alternatively, a radiolabeled compound of the inventioncan be prepared by linking a compound of formula (I) to a chelatinggroup that includes a detectable radionuclide (e.g., metallicradionuclide). Such compounds can be useful to image tissues with MMPactivity or tumors, in vivo or in vitro.

[0108] As used herein, a “chelating group” is a group that can include adetectable radionuclide (e.g., a metallic radioisotope). Any suitablechelating group can be employed. Suitable chelating groups aredisclosed, e.g., in Poster Sessions, Proceedings of the 46th AnnualMeeting, J. Nuc.Med., p. 316, No. 1386; Scientific Papers, Proceedingsof the 46th Annual Meeting, J. Nuc.Med., p. 123, No. 499; ScientificPapers, Proceedings of the 46th Annual Meeting, J. Nuc.Med., p. 102, No.413; Scientific Papers, Proceedings of the 46th Annual Meeting, J.Nuc.Med., p. 102, No. 414; Scientific Papers, Proceedings of the 46thAnnual Meeting, J. Nuc.Med., p. 103, No. 415; Poster Sessions,Proceedings of the 46th Annual Meeting, J. Nuc.Med., p. 318, No. 1396;Poster Sessions, Proceedings of the 46th Annual Meeting, J. Nuc.Med., p.319, No. 1398; M. Moi et al., J. Amer. Chem., Soc., 49, 2639 (1989); S.V. Deshpande et al., J. Nucl. Med., 31, 473 (1990); G. Kuser et al.,Bioconj. Chem., 1, 345 (1990); C. J. Broan et al., J. C. S. Chem. Comm.,23, 1739 (1990); C. J. Anderson et al., J. Nucl. Med. 36, 850 (1995);U.S. Pat. No. 5,739,313; and U.S. Pat. No. 6,004,533. Specifically, thechelating group can be.

[0109] As used herein, a “detectable radionuclide” is any suitableradionuclide (i.e., radioisotope) useful in a diagnostic procedure invivo or in vitro. Suitable detectable radionuclides include metallicradionuclides (i.e., metallic radioisotopes) and non-metallicradionuclides (i.e., non-metallic radioisotopes).

[0110] Suitable metallic radionuclides (i.e., metallic radioisotopes ormetallic paramagnetic ions) include Antimony-124, Antimony-125,Arsenic-74, Barium-103, Barium-140, Beryllium-7, Bismuth-206,Bismuth-207, Cadmium-109, Cadmium-1 15m, Calcium-45, Cerium-139,Cerium-141, Cerium-144, Cesium-137, Chromium-51, Cobalt-55, Cobalt-56,Cobalt-57, Cobalt-58, Cobalt-60, Cobalt-64, Copper-67, Erbium-169,Europium-152, Gallium-64, Gallium-68, Gadolinium-153, Gadolinium-157Gold-195, Gold-199, Hafnium-175, Hafnium-175-181, Holmium-166,Indium-110, Indium-111, Iridium-192, Iron-55, Iron-59, Krypton-85,Lead-210, Manganese-54, Mercury-1 97, Mercury-203, Molybdenum-99,Neodymium-147, Neptunium-237, Nickel-63, Niobium-95, Osmium-185+191,Palladium-103, Platinum-195m, Praseodymium-143, Promethium-147,Protactinium-233, Radium-226, Rhenium-186, Rhenium-188, Rubidium-86,Ruthenium-103, Ruthenium-106, Scandium-44, Scandium-46, Selenium-75,Silver-110m, Silver-111, Sodium-22, Strontium-85, Strontium-89,Strontium-90, Sulfur-35, Tantalum-182, Technetium-99m, Tellurium-125,Tellurium-132, Thallium-204, Thorium-228, Thorium-232, Thallium-170,Tin-113, Tin-114, Tin-117m, Titanium-44, Tungsten-185, Vanadium-48,Vanadium-49, Ytterbium-169, Yttrium-86, Yttrium-88, Yttrium-90,Yttrium-91, Zinc-65, and Zirconium-95.

[0111] Specifically, the chelating group can include more than onemetallic radioisotope. More specifically, the detectable chelating groupcan include 2 to about 10, 2 to about 8, 2 to about 6, or 2 to about 4metallic radioisotopes.

[0112] Specifically, the non-metallic radionuclide can be a non-metallicparamagnetic atom (e.g., Fluorine-19); or a non-metallic positronemitting radionuclide (e.g., Carbon-11, Fluorine-18, Iodine-123, orBromine-76).

[0113] Specifically, the compounds of the present invention can includemore than one non-metallic radioisotope. More specifically, thecompounds of the present invention can include 2 to about 10, 2 to about8, 2 to about 6, or 2 to about 4 non-metallic radioisotopes.

[0114] A compound of formula (I), or a pharmaceutically acceptable saltthereof, can be administered to a mammal (e.g., human) in conjunctionwith a chemotherapeutic agent, or a pharmaceutically acceptable saltthereof. Accordingly, a compounds of formula (I) can be administered inconjunction with a chemotherapeutic agent to treat a tumor or cancer.

[0115] As used herein, a “chemotherapeutic agent” is a compound that hasbiological activity against one or more forms of cancer and can beadministered to a patient with a compound of formula (I) without losingits anticancer activity. Suitable chemotherapeutic agents include, e.g.,antineoplasts. Representative antineoplasts include, e.g., adjuncts,androgen inhibitors, antibiotic derivatives, antiestrogens,antimetabolites, cytotoxic agents, hormones, immunomodulators, nitrogenmustard derivatives and steroids. Physicians' Desk Reference, 50thEdition, 1996.

[0116] Representative adjuncts include, e.g., levamisole, galliumnitrate, granisetron, sargramostim strontium-89 chloride, filgrastim,pilocarpine, dexrazoxane, and ondansetron. Physicians' Desk Reference,50th Edition, 1996.

[0117] Representative androgen inhibitors include, e.g., flutamide andleuprolide acetate. Physicians' Desk Reference, 50th Edition, 1996.

[0118] Representative antibiotic derivatives include, e.g., doxorubicin,bleomycin sulfate, daunorubicin, dactinomycin, and idarubicin.

[0119] Representative antiestrogens include, e.g., tamoxifen citrate andanalogs thereof. Physicians' Desk Reference, 50th Edition, 1996.Additional antiestrogens include nonsteroidal antiestrogens such astoremifene, droloxifene and roloxifene. Magarian et al., CurrentMedicinal Chemistry, 1994, Vol. 1, No. 1.

[0120] Representative antimetabolites include, e.g., fluorouracil,fludarabine phosphate, floxuridine, interferon alfa-2b recombinant,methotrexate sodium, plicamycin, mercaptopurine, and thioguanine.Physicians' Desk Reference, 50th Edition, 1996.

[0121] Representative cytotoxic agents include, e.g., doxorubicin,carmustine [BCNU], lomustine [CCNU], cytarabine USP, cyclophosphamide,estramucine phosphate sodium, altretamine, hydroxyurea, ifosfamide,procarbazine, mitomycin, busulfan, cyclophosphamide, mitoxantrone,carboplati, cisplati, cisplatin, interferon alfa-2a recombinant,paclitaxel, teniposide, and streptozoci. Physicians' Desk Reference,50th Edition, 1996.

[0122] Representative hormones include, e.g., medroxyprogesteroneacetate, estradiol, megestrol acetate, octreotide acetate,diethylstilbestrol diphosphate, testolactone, and goserelin acetate.Physicians' Desk Reference, 50th Edition, 1996.

[0123] Representative immunodilators include, e.g., aldesleukin.Physicians' Desk Reference, 50th Edition, 1996.

[0124] Representative nitrogen mustard derivatives include, e.g.,melphalan, chlorambucil, mechlorethamine, and thiotepa. Physicians' DeskReference, 50th Edition, 1996.

[0125] Representative steroids include, e.g., betamethasone sodiumphosphate and betamethasone acetate. Physicians' Desk Reference, 50thEdition, 1996.

[0126] Additional suitable chemotherapeutic agents include, e.g.,alkylating agents, antimitotic agents, plant alkaloids, biologicals,topoisomerase I inhibitors, topoisomerase II inhibitors, synthetics,antiangiogenic drugs, and antibodies. See, e.g., AntiCancer Agents byMechanism,http://www.dtp.nci.nih.gov/docs/cancer/searches/standard_mechanism_list.html,Apr. 12, 1999; Approved Anti-Cancer Agents,http://www.ctep.info.nih.gov/handbook/HandBookText/fda_agen.htm, pages1-7, Jun. 18, 1999; MCMP 611 Chemotherapeutic Drugs to Know,http//www.vet.purdue.edu/depts/bms/courses/mcmp611/chrx/drg2no61.html,Jun. 24, 1999; Chemotherapy,http://www.vetmed.1su.edu/oncology/Chemotherapy.htm, Apr. 12, 1999; andAngiogenesis Inhibitors in Clinical Trials,http://www.cancertrials.nci.nih.gov/news/angio/table.html, pages 1-5,Apr. 19, 2000.

[0127] Representative alkylating agents include, e.g., asaley, AZQ,BCNU, busulfan, bisulphan, carboxyphthalatoplatinum, CBDCA, CCNU, CHIP,chlorambucil, chlorozotocin, cis-platinum, clomesone,cyanomorpholinodoxorubicin, cyclodisone, cyclophosphamide,dianhydrogalactitol, fluorodopan, hepsulfam, hycanthone, iphosphamide,melphalan, methyl CCNU, mitomycin C, mitozolamide, nitrogen mustard,PCNU, piperazine, piperazinedione, pipobroman, porfiromycin,spirohydantoin mustard, streptozotocin, teroxirone, tetraplatin,thiotepa, triethylenemelamine, uracil nitrogen mustard, and Yoshi-864.AntiCancer Agents by Mechanism,http://dtp.nci.nih.gov/docs/cancer/searches/standard_mechanismlist.html, Apr. 12, 1999.

[0128] Representative antimitotic agents include, e.g., allocolchicine,Halichondrin B, colchicine, colchicine derivatives, dolastatin 10,maytansine, rhizoxin, paclitaxel derivatives, paclitaxel,thiocolchicine, trityl cysteine, vinblastine sulfate, and vincristinesulfate. AntiCancer Agents by Mechanism,http://dtp.nci.nih.gov/docs/cancer/searches/standard_mechanism_list.html,Apr. 12, 1999.

[0129] Representative plant alkaloids include, e.g., actinomycin D,bleomycin, L-asparaginase, idarubicin, vinblastine sulfate, vincristinesulfate, mitramycin, mitomycin, daunorubicin, VP-16-213, VM-26,navelbine and taxotere. Approved Anti-Cancer Agents,http://ctep.info.nih.gov/handbook/HandBookText/fda_agent.htm, Jun. 18,1999.

[0130] Representative biologicals include, e.g., alpha interferon, BCG,G-CSF, GM-CSF, and interleukin-2. Approved Anti-Cancer Agents,http://ctep.info.nih.gov/handbook/HandBookText/fda_agent.htm, Jun. 18,1999.

[0131] Representative antiangiogenic drugs include e.g., marimastat,AG3340, COL-3, neovastat, BMS-275291, TNP-470, thalidomide, squalamine,combretastatin A-4 prodrug, endostatin, SU5416, SU6668,interferon-alpha, anti-VEGF antibody, EMD121974, CAI, interleukin-12,and IM862. Angiogenesis Inhibitors in Clinical Trials,http://www.cancertrials.nci.nih.gov/news/angio/table.html, pages 1-5,Apr. 19, 2000.

[0132] Representative topoisomerase I inhibitors include, e.g.,camptothecin, camptothecin derivatives, and morpholinodoxorubicin.AntiCancer Agents by Mechanism,http://dtp.nci.nih.gov/docs/cancer/searches/standard_mechanism_list.html, Apr. 12, 1999.

[0133] Additional biologicals include drugs designed to inhibit tumorvascularization, which is also known as tumor angiogenesis. These drugscan be potent antiangiogenic agents. Additional biologicals includehumanized antibodies to growth factors, for example, to HER2, signalingmolecules and adhesion receptors. Additional biologicals also includetreatment with recombinant viruses and other means of gene therapydelivery, including for example, DNA, oligonucleotides, rybozymes, andliposomes.

[0134] Representative topoisomerase II inhibitors include, e.g.,mitoxantron, amonafide, m-AMSA, anthrapyrazole derivatives,pyrazoloacridine, bisantrene HCL, daunorubicin, deoxydoxorubicin,menogaril, N, N-dibenzyl daunomycin, oxanthrazole, rubidazone, VM-26 andVP-16. AntiCancer Agents by Mechanism,http://dtp.nci.nih.gov/docs/cancer/searches/standard_mechanism_list.html,Apr. 12, 1999.

[0135] Representative synthetics include, e.g., hydroxyurea,procarbazine, o,p′-DDD, dacarbazine, CCNU, BCNU,cis-diamminedichloroplatimun, mitoxantrone, CBDCA, levamisole,hexamethylmelamine, all-trans retinoic acid, gliadel and porfimersodium. Approved Anti-Cancer Agents, http://ctep.info.nih.gov/handbook/HandBookText/fda_agen.htm, Jun. 18, 1999.

[0136] In cases where compounds are sufficiently basic or acidic to formstable nontoxic acid or base salts, administration of the compounds assalts may be appropriate. Examples of pharmaceutically acceptable saltsare organic acid addition salts formed with acids which form aphysiological acceptable anion, for example, tosylate, methanesulfonate,acetate, citrate, malonate, tartarate, succinate, benzoate, ascorbate,α-ketoglutarate, and α-glycerophosphate. Suitable inorganic salts mayalso be formed, including hydrochloride, sulfate, nitrate, bicarbonate,and carbonate salts.

[0137] Pharmaceutically acceptable salts may be obtained using standardprocedures well known in the art, for example by reacting a sufficientlybasic compound such as an amine with a suitable acid affording aphysiologically acceptable anion. Alkali metal (e.g., sodium, potassiumor lithium) or alkaline earth metal (e.g., calcium) salts of carboxylicacids can also be made.

[0138] The compounds of formula (I) can be formulated as pharmaceuticalcompositions and administered to a mammalian host, such as a humanpatient in a variety of forms adapted to the chosen route ofadministration, i.e., orally or parenterally, by intravenous,intramuscular, topical or subcutaneous routes.

[0139] Thus, the present compounds may be systemically administered,e.g., orally, in combination with a pharmaceutically acceptable vehiclesuch as an inert diluent or an assimilable edible carrier. They may beenclosed in hard or soft shell gelatin capsules, may be compressed intotablets, or may be incorporated directly with the food of the patient'sdiet. For oral therapeutic administration, the active compound may becombined with one or more excipients and used in the form of ingestibletablets, buccal tablets, troches, capsules, elixirs, suspensions,syrups, wafers, and the like. Such compositions and preparations shouldcontain at least 0.1% of active compound. The percentage of thecompositions and preparations may, of course, be varied and mayconveniently be between about 2 to about 60% of the weight of a givenunit dosage form. The amount of active compound in such therapeuticallyuseful compositions is such that an effective dosage level will beobtained.

[0140] The tablets, troches, pills, capsules, and the like may alsocontain the following: binders such as gum tragacanth, acacia, cornstarch or gelatin; excipients such as dicalcium phosphate; adisintegrating agent such as corn starch, potato starch, alginic acidand the like; a lubricant such as magnesium stearate; and a sweeteningagent such as sucrose, fructose, lactose or aspartame or a flavoringagent such as peppermint, oil of wintergreen, or cherry flavoring may beadded. When the unit dosage form is a capsule, it may contain, inaddition to materials of the above type, a liquid carrier, such as avegetable oil or a polyethylene glycol. Various other materials may bepresent as coatings or to otherwise modify the physical form of thesolid unit dosage form. For instance, tablets, pills, or capsules may becoated with gelatin, wax, shellac or sugar and the like. A syrup orelixir may contain the active compound, sucrose or fructose as asweetening agent, methyl and propylparabens as preservatives, a dye andflavoring such as cherry or orange flavor. Of course, any material usedin preparing any unit dosage form should be pharmaceutically acceptableand substantially non-toxic in the amounts employed. In addition, theactive compound may be incorporated into sustained-release preparationsand devices.

[0141] The active compound may also be administered intravenously orintraperitoneally by infusion or injection. Solutions of the activecompound or its salts can be prepared in water, optionally mixed with anontoxic surfactant. Dispersions can also be prepared in glycerol,liquid polyethylene glycols, triacetin, and mixtures thereof and inoils. Under ordinary conditions of storage and use, these preparationscontain a preservative to prevent the growth of microorganisms.

[0142] The pharmaceutical dosage forms suitable for injection orinfusion can include sterile aqueous solutions or dispersions or sterilepowders comprising the active ingredient which are adapted for theextemporaneous preparation of sterile injectable or infusible solutionsor dispersions, optionally encapsulated in liposomes. In all cases, theultimate dosage form should be sterile, fluid and stable under theconditions of manufacture and storage. The liquid carrier or vehicle canbe a solvent or liquid dispersion medium comprising, for example, water,ethanol, a polyol (e.g., glycerol, propylene glycol, liquid polyethyleneglycols, and the like), vegetable oils, nontoxic glyceryl esters, andsuitable mixtures thereof. The proper fluidity can be maintained, forexample, by the formation of liposomes, by the maintenance of therequired particle size in the case of dispersions or by the use ofsurfactants. The prevention of the action of microorganisms can bebrought about by various antibacterial and antifungal agents, forexample, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, andthe like. In many cases, it will be preferable to include isotonicagents, for example, sugars, buffers or sodium chloride. Prolongedabsorption of the injectable compositions can be brought about by theuse in the compositions of agents delaying absorption, for example,aluminum monostearate and gelatin.

[0143] Sterile injectable solutions are prepared by incorporating theactive compound in the required amount in the appropriate solvent withvarious of the other ingredients enumerated above, as required, followedby filter sterilization. In the case of sterile powders for thepreparation of sterile injectable solutions, the preferred methods ofpreparation are vacuum drying and the freeze drying techniques, whichyield a powder of the active ingredient plus any additional desiredingredient present in the previously sterile-filtered solutions.

[0144] For topical administration, the present compounds may be appliedin pure form, i.e., when they are liquids. However, it will generally bedesirable to administer them to the skin as compositions orformulations, in combination with a dermatologically acceptable carrier,which may be a solid or a liquid.

[0145] Useful solid carriers include finely divided solids such as talc,clay, microcrystalline cellulose, silica, alumina and the like. Usefulliquid carriers include water, alcohols or glycols orwater-alcohol/glycol blends, in which the present compounds can bedissolved or dispersed at effective levels, optionally with the aid ofnon-toxic surfactants. Adjuvants such as fragrances and additionalantimicrobial agents can be added to optimize the properties for a givenuse. The resultant liquid compositions can be applied from absorbentpads, used to impregnate bandages and other dressings, or sprayed ontothe affected area using pump-type or aerosol sprayers.

[0146] Thickeners such as synthetic polymers, fatty acids, fatty acidsalts and esters, fatty alcohols, modified celluloses or modifiedmineral materials can also be employed with liquid carriers to formspreadable pastes, gels, ointments, soaps, and the like, for applicationdirectly to the skin of the user.

[0147] Examples of useful dermatological compositions which can be usedto deliver the compounds of formula I to the skin are known to the art;for example, see Jacquet et al. (U.S. Pat. No. 4,608,392), Geria (U.S.Pat. No. 4,992,478), Smith et al. (U.S. Pat. No. 4,559,157) and Wortzman(U.S. Pat. No. 4,820,508).

[0148] Useful dosages of the compounds of formula I can be determined bycomparing their in vitro activity, and in vivo activity in animalmodels. Methods for the extrapolation of effective dosages in mice, andother animals, to humans are known to the art; for example, see U.S.Pat. No. 4,938,949.

[0149] Generally, the concentration of the compound(s) of formula I in aliquid composition, such as a lotion, will be from about 0.1-25 wt-%,preferably from about 0.5-10 wt-%. The concentration in a semi-solid orsolid composition such as a gel or a powder will be about 0.1-5 wt-%,preferably about 0.5-2.5 wt-%.

[0150] The amount of the compound, or an active salt or derivativethereof, required for use in treatment will vary not only with theparticular salt selected but also with the route of administration, thenature of the condition being treated and the age and condition of thepatient and will be ultimately at the discretion of the attendantphysician or clinician.

[0151] In general, however, a suitable dose will be in the range of fromabout 0.5 to about 100 mg/kg, e.g., from about 10 to about 75 mg/kg ofbody weight per day, such as 3 to about 50 mg per kilogram body weightof the recipient per day, preferably in the range of 6 to 90 mg/kg/day,most preferably in the range of 15 to 60 mg/kg/day.

[0152] The compound is conveniently administered in unit dosage form;for example, containing 5 to 1000 mg, conveniently 10 to 750 mg, mostconveniently, 50 to 500 mg of active ingredient per unit dosage form.

[0153] Ideally, the active ingredient should be administered to achievepeak plasma concentrations of the active compound of from about 0.5 toabout 75 μM, preferably, about 1 to 50 μM, most preferably, about 2 toabout 30 μM. This may be achieved, for example, by the intravenousinjection of a 0.05 to 5% solution of the active ingredient, optionallyin saline, or orally administered as a bolus containing about 1-100 mgof the active ingredient. Desirable blood levels may be maintained bycontinuous infusion to provide about 0.01-5.0 mg/kg/hr or byintermittent infusions containing about 0.4-15 mg/kg of the activeingredient(s).

[0154] The desired dose may conveniently be presented in a single doseor as divided doses administered at appropriate intervals, for example,as two, three, four or more sub-doses per day. The sub-dose itself maybe further divided, e.g., into a number of discrete loosely spacedadministrations; such as multiple inhalations from an insufflator or byapplication of a plurality of drops into the eye.

[0155] The ability of a compound of the invention to act as an MMPinhibitor may be determined using pharmacological models which are wellknown to the art, or using the methods described hereinbelow.

[0156] Fluorescence Enzymatic Activity Assays

[0157] The enzymatic activity of MMP-2, MMP-9, and MMP-7 was monitoredwith the fluorescence quenched substrate MOCAcPLGLA₂pr(Dnp)-AR-NH₂.Fluorescence was measured with a Photon Technology International (PTI)spectrofluorometer interfaced to a Pentium computer, equipped with theRatioMaster™ and FeliX™ hardware and software, respectively. The cuvettecompartment was thermostated at 25.0° C. Substrate hydrolysis wasmonitored at emission and excitation wavelengths of 328 and 393 nm andexcitation and emission band passes of 1 and 3 nm, respectively.Fluorescence measurements were taken every 4 s. Less than 10% hydrolysisof the fluorogenic substrate was monitored, as described by Knight.Knight, C. G. Methods Enzymol. 1995, 248, 18-34. Stromelysin 1 enzymaticactivity was monitored using the synthetic fluorogenic substrateMOCAcRPKPVE-Nva-WRK(Dnp)-NH₂ (Peptides International, Louisville, Ky.)at excitation and emission wavelengths of 325 and 393 nm and excitationand emission band passes of 1 and 3 nm, respectively.

[0158] Enzymes and Protein Inhibitors.

[0159] Human pro-MMP-2, pro-MMP-9, TIMP-1 and TIMP-2 were expressed inHeLa S3 cells infected with the appropriate recombinant vaccinia virusesand were purified to homogeneity, as previously described. Fridman, R.;Fuerst, T. R.; Bird, R. E.; Hoyhtya, M.; Oelkuct, M.; Kraus, S.;Komarek, D.; Liotta, L. A.; Berman, M. L.; Stetler-Stevenson, W. G. J.Biol. Chem. 1992, 267, 15398-15405. Fridman, R.; Birs, R. E.; Hoyhtya,M.; Oelkuct, M.; Komarek, D.; Liang, C. M.; Berman, M. L.; Liotta, L.A.; Stetler-Stevenson, W. G.,; Fuerst, T. R. Biochem. J. 1993, 289,411-416. Pro-MMP-2, pro-MMP-9, TIMP-1 and TIMP-2 concentrations weredetermined using the extinction coefficients of 122,800, 114,360, 26,500and 39,600 M⁻¹cm⁻¹, respectively. To obtain active MMP-2, pro-MMP-2 (7.3μM) was incubated at 37° C. for 1 h with 1 mM p-aminophenylmercuricacetate (APMA) (dissolved in 200 mM Tris) in buffer C. The enzymesolution was dialyzed against buffer D at 4° C. to remove APMA. ActiveMMP-9 was obtained by incubating pro-MMP-9 (1 μM) with heat-activatedrecombinant human stromelysin 1 (68 nM) (MMP-3, generously provided byDr. Paul Cannon, Center for Bone and Joint Research, Palo Alto, Calif.)at 37° C., for 2.5 h in buffer C.

[0160] The resulting solution was subjected to gelatin-agarosechromatography to remove stromelysin 1. MMP-9 was eluted with buffer Dcontaining 10% DMSO and dialyzed against the same buffer without DMSO toremove the organic solvent. Pro-MMP-2 and pro-MMP-9 activation reactionswere monitored using the fluorescence quenched substrateMOCAcPLGLA₂pr(Dnp)-AR-NH₂ (Peptides International, Louisville, Ky.), aswill be described below. The MMP-2 and MMP-9 concentrations weredetermined by titration with TIMP-1.

[0161] Kinetic Analyses.

[0162] Progress curves were obtained by adding enzyme (0.5-2 nM) to amixture of fluorogenic substrate (5-7 μM) and varying concentrations ofinhibitor in buffer R containing 5-15% DMSO (final volume 2 ml), inacrylic cuvettes with stirring and monitoring the increase influorescence with time for 15-30 minutes. The progress curves werenonlinear least squares fitted to Equation 1 (Muller-Steffner, H. M.,Malver, O., Hosie, L., Oppenheimer, N. J., and Schuber, F. J. Biol.Chem. 1992, 267, 9606-9611.):

F=v _(s) t+I(v _(o) −v _(s))(1−exp(−kt))/k+F ₀  (1)

[0163] where v_(o) represents the initial rate, v_(s), the steady staterate, k, the apparent first order rate constant characterizing theformation of the steady-state enzyme-inhibitor complex and F_(o), theinitial fluorescence, using the program SCIENTIST (MicroMath ScientificSoftware, Salt Lake City, Utah). The obtained k values, v₀ and v_(s)were further analyzed according to Equations 2 and 3 for a one-stepassociation mechanism

k=k _(off) +k _(on) [I]/(1+[S]/Km)  (2)

(v_(o) −v _(s))/v_(s) =[I]/(K _(i)(1+[S]/K _(m)))  (3)

[0164] Intercept and slope values, obtained by linear regression of thek versus inhibitor concentration plot (Equation 2), yielded theassociation and dissociation rate constants k_(on) and k_(off),respectively, and the inhibition constant K_(i) (k_(off)/k_(on)).Alternatively, K_(i) was determined from the slope of the (v_(o) −v_(s))/v_(s)vs [I] plot according to Equation 3.

[0165] The dissociation rate constants were determined independentlyfrom the enzyme activity recovered after dilution of a pre-formedenzyme-inhibitor complex. To this end, typically 200 nM of enzyme wasincubated with 1 μM of inhibitor for a sufficient time to reachequilibrium (>45 min) at 25.0° C. The complex was diluted into 2 mL ofbuffer R containing fluorogenic substrate (5-7 μM final concentration)to a final enzyme concentration of 1 nM. Recovery of enzyme activity wasmonitored for ˜30 min. The fluorescence versus time trace was fitted,using the program SCIENTIST, to Equation 4

F=v _(s) t+(v _(o) −v _(s))(1−exp(−k _(off)))/k _(off) +F ₀  (4)

[0166] where v_(o) represents the initial rate (very small), v_(s), therate observed when the E.I complex is completely dissociated andk_(off), the first order rate constant when the E.I dissociation.

[0167] Analysis for linear competitive inhibition was performed in thefollowing manner. Initial rates were obtained by adding enzyme (0.5-2nM) to a mixture of fluorogenic substrate (5-7 μM) and varyingconcentrations of inhibitor in buffer R, containing 5-15% DMSO (finalvolume 1 mL) in semi-micro quartz cuvettes, and monitoring the increasein fluorescence with time for 5-10 minutes. The fluorescence versus timetraces were fitted by linear regression analysis using FeliX™. Theinitial rates were fitted to Equation 5 (Segel, I. H. in: EnzymeKinetics, Wiley Inc., New York, 1975, pp. 104.):

v/V _(max) =S/(K _(m)(1+I/K _(i))+S)  (5)

[0168] where v and V_(max) represent the initial and maximal velocities,S and I, the substrate and inhibitor concentrations, respectively, K_(m)the Michaelis-Menten constant for the substrate-enzyme reaction andK_(i) the inhibition constant, using the program SCIENTIST.

[0169] Inhibitors 1-4 all bind with the active site of the MMPs thatwere used in the study, with K_(i) values of micromolar, or less,however, the behavior of inhibitor 1 was very different. Inhibitor 1showed a dual behavior. It served as a mechanism-based inhibitor with apartition ratio of 79±10 (i.e. k_(cat)/k_(inact)) for MMP-2 and 416±63for MMP-9. Furthermore, it also behaved as a slow-binding inhibitor, forwhich the rate constants for the on-set of inhibition (k_(on)) andrecovery of activity from inhibition (k_(off)) were evaluated (Table 1).It would appear that coordination of the thiirane with the zinc ion (asseen in energy-minimized computational models; FIG. 1) would set inmotion a confornational change, which is presumed from the slow-bindingkinetic behavior. The kinetic data fit the model for slow-bindinginhibition. Morrison, J. F. Adv. Enzymol. 1988, 61, 201-301. Covalentmodification of the enzymes results from this conformational change.Inhibitor 1 was incubated with MMP-2 to the point that less than 5%activity remained. This inhibitor-enzyme complex was dialyzed over threedays, which resulted in recovery of approximately 50% of the activity.This observation is consistent with modification of the active siteGlu-404 (according to the numbering for human MMP-2), via the formationof an ester bond, which is a relatively labile covalent linkage. Thetime-dependent loss of activity is not merely due to the slow-bindingbehavior. For instance, for a k_(off) of 2×10⁻³ s⁻¹ (the values are notvery different from one another in Table 1) the half time for recoveryof activity (t_(½)) is calculated at just under 6 min. The fact that 50%of activity still did not recover after dialysis over three daysstrongly argues for the covalency of enzyme modification.

[0170] Selectivity in inhibition of gelatinases by inhibitor 1 wasobserved. Its K_(i) values are 13.9±4 nM and 600±200 nM for MMP-2 andMMP-9, respectively. The corresponding K_(i) values are elevated to themicromolar range for the other MMPs, even for the case of MMP-3, whichdoes show the slow-binding, mechanism-based inhibition profile. Inaddition, the values for k_(on) are 611- and 78-fold larger for MMP-2and MMP-9, respectively, than that for MMP-3. Whereas the k_(off) valuesare more similar to one another, the value for MMP-2 is the smallest, sothe reversal of inhibition of this enzyme takes place more slowly.Collectively, these kinetic parameters demonstrate that inhibitor 1 canbe a potent and selective inhibitor for MMP-2, MMP-9, and especiallyMMP-2. It has been previously shown that two molecules of either TIMP-1or TIMP-2 (endogenous cellular protein inhibitors of MMPs) bind toactivated MMP-2 and MMP-9. Olson, M. W.; Gervasi, D. C.; Mobashery, S.;Fridman, R. J. Biol. Chem. 1997, 272, 29975. One binding event is highaffinity and would appear physiologically relevant, whereas the secondbinding event takes place with relatively lower affinity (micromolar).Olson, M. W.; Gervasi, D. C.; Mobashery, S.; Fridman, R. J. Biol. Chem.1997, 272, 29975. Inhibition of MMP-2 and MMP-9 by TIMPs also followsslow-binding kinetics. The kinetic parameters for these interactions atthe high affinity site are listed in Table 1. The kinetic parameters forthe slow-binding component of inhibition of MMP-2 and MMP-9 by inhibitor1 (K_(on) and K_(off)) approach closely the same parameters for those ofthe protein inhibitors. Olson, M. W.; Gervasi, D. C.; Mobashery, S.;Fridman, R. J. Biol. Chem. 1997, 272, 29975-29983.

[0171] Oxiranes 4-6 inhibit MMPs in a competitive manner with higherK_(i) values. There was no evidence of slow-binding behavior ortime-dependence of loss of activity with this inhibitor with any of theMMPs.

[0172] Small-molecule inhibitor 1 follows both slow-binding andmechanism-based inhibition in its kinetic profile. This compound appearsto behave very similarly to the endogenous cellular protein inhibitorsfor MMPs (TIMPs) in the slow-binding component of inhibition.Furthermore, the inhibitor also exhibits a covalent mechanism-basedbehavior in inhibition of these enzymes. The high discrimination intargeting that inhibitor 1 displays (both in affinities and the modes ofinhibition) among the other structurally similar MMPs is noteworthy andcould serve as a paradigm in the design of inhibitors for other closelyrelated enzymes in the future.

EXAMPLES

[0173] Experimental Procedures

[0174]¹H and ¹³C NMR spectra were recorded on either a VarianGemini-300, a Varian Mercury-400 or a Varian Unity-500 spectrometer.Chemical shifts are reported in ppm from tetramethylsilane on the δscale. Infrared spectra were recorded on a Nicolet 680 DSPspectrophotometer. Mass spectra were recorded on a Kratos MS 8ORFTspectrometer. Melting points were taken on an Electrothermal meltingpoint apparatus and are uncorrected. Thin-layer chromatography wasperformed with Whatman reagents 0.25 mm silica gel 60-F plates. Allother reagents were purchased from either Aldrich Chemical Company orAcross Organics.

[0175] The following buffers were used in experiments with enzymes:Buffer C (50 mM HEPES at pH 7.5, 150 mM NaCl, 5 mM CaCl₂, 0.02%Brij-35); buffer R (50 mM HEPES at pH 7.5, 150 mM NaCl, 5 mM CaCl₂,0.01% Brij-35, and 1% v/v Me₂SO) and buffer D (50 mM Tris at pH 7.5, 150mM NaCl, 5 mM CaCl₂, and 0.02% Brij-35).

Example 1

[0176] (4-Phenoxyphenylsulfonyl)methyloxirane (4).

[0177] To compound 11 (598 mg, 2.5 mmol) in dichloromethane (10 mL),mCPBA (2.84 g, 10 mmol, Aldrich 57-86%), was slowly added. The mixturewas stirred at room temperature for 3 days, after which time a secondportion of mCPBA (2.84 g, 10 mmol) was added. The mixture was thenstirred for another 4 days, after which time the mixture was poured intoethyl acetate (200 mL), and washed with aqueous sodium thiosulfate (3×50mL, 10% w/v), aqueous sodium bicarbonate (3×50 ml, 5% w/v), and brine(50 ml). The organic phase was dried over magnesium sulfate and wasconcentrated to provide a yellow oil. The crude material was purified bycolumn chromatography (silica, 4:1 hexanes:ethyl acetate) to givecompound 4 as a pale yellow semi-solid (501 mg, 70%). ¹H NMR (500 MHz,CDCl₃) δ 7.90-7.86 (m, 2H), 7.46-7.40 (m, 2H), 7.26-7.22 (m, 1H),7.10-6.96 (m, 4H), 3.34-3.24 (m, 2H), 2.84-2.80 (m, 1H), 2.49-2.46 (m,1H); ¹³C NMR (125 MHz, CDCl₃) δ 163.15, 154.95, 130.76, 130.51, 125.52,120.77, 117.83, 59.89, 46.13; IR(film) 3054 (w), 2919 (w), 1576 (s),1492 (s), 1320 (s), 1245 (s), 1148 (s) cm⁻¹; m/z (EI) 290 (M⁺, 100%),233 (70), 217 (50), 185 (40); HRMS (EI) calcd. for C₁₅H₁₄O₄S 290.0613,found 290.0611.

[0178] The intermediate, compound 11, was prepared as follows:

[0179] (A.) O-4-Phenoxyphenyl-N,N-dimethylthiocarbamate (8).

[0180] To a solution of 4-phenoxyphenol (7, 8.46 g, 45 mmol) in DMF (40mL) at 10° C., sodium hydride (1.83 g, 45 mmol, 60% dispersion inmineral oil) was added in small portions. After the evolution ofhydrogen ceased, N,N-dimethylthiocarbamoyl chloride (6.16 g, 50 mmol)was added in one portion. The reaction mixture was then stirred at 70°C. for 2 hours. The mixture was cooled to room temperature, poured intowater (100 mL) and extracted with chloroform (3×50 mL). The combinedorganic extracts were washed with aqueous potassium hydroxide (50 mL, 5%w/v), and brine (10×50 mL). The organic extract was dried over magnesiumsulfate and concentrated to obtain a yellow oil. The crude material waspurified by column chromatography (silica, 5:1 hexanes:ethyl acetate) togive compound 8 as a white solid (11.16 g, 90%). m.p. 50-51° C.; ¹H NMR(300 MHz, CDCl₃) δ 7.38-7.31 (m, 2H), 7.14-7.08 (m, 1H), 7.06-7.00 (m,6H), 3.46 (s, 3H), 3.34 (s, 3H); ¹³C NMR (75 MHz, CDCl₃) δ 188.17,157.26, 155.16, 149.62, 130.05, 124.11, 123.71, 119.31, 43.57, 38.96; IR(KBr) 3040 (m), 2938 (s), 1587 (s), 1487 (s), 1394 (s), 1287 (s), 1190(s) cm⁻¹; m/z (EI) 273 (M⁺, 15%), 186 (100); HRMS (EI) calcd. forC₁₅H,₅NO₂S 273.0823, found 273.0824.

[0181] (B.) S-4-Phenoxyphenyl-N,N-dimethylthiocarbamate (9).

[0182] Compound 8 (3.99 g, 15 mmol) was heated under argon at 260° C.for 3.5 hours. The resulting dark brown oil was purified by columnchromatography using a gradient eluent system (silica, 19:1 then 9:1then 3:1 hexanes:ethyl acetate) to obtain compound 9 as a pale yellowsolid (2.55 g, 64%). m.p. 97-99° C.; ¹H NMR (400 MHz, CDCl₃) δ 7.45-7.40(m, 2H), 7.40-7.30 (m, 2H), 7.15-7.10 (m, 1H), 7.05 (d, J=8.8 Hz, 2H)6.98 (d, J=8.8 Hz, 2H) 3.08 (bs, 3H), 3.02 (bs, 3H); ¹³C NMR (100 MHz,CDCl₃) δ 167.48, 158.87, 156.53, 137.66, 130.09, 124.14, 122.39, 119.87,118.94,37.14; IR(KBr) 3037 (w), 2925 (w), 1652 (s), 1581 (s) 1486 (s),1239 (s) cm⁻¹; m/z (EI) 273 (M⁺, 25%), 257 (5), 200 (5); HRMS (EI)calcd. for C₁₅H₁₅NO₂S 273.0823, found 273.0822.

[0183] (C.) 4-Phenoxythiophenol (10).

[0184] A mixture of compound 9 (2.55 g, 9 mmol) in methanol (20 mL), andaqueous NaOH (10 mL, 10% w/v), were refluxed for 4 hours. The solutionwas cooled to room temperature and was acidified to pH 1 with aqueousHCl (1M). Water (100 mL) was added and the mixture was extracted withchloroform (3×50 mL). The combined organic extracts were washed withbrine (50 mL), dried over magnesium sulfate and concentrated to obtain ayellow oil. The crude product was purified by column chromatography(silica, 5:1 hexanes:ethyl acetate) to give compound 10 as a pale yellowoil (1.80 g, >99%). 1H NMR (300 MHz, CDCl₃) δ 7.36-7.31 (m, 2H),7.30-7.25 (m, 2H), 7.13-7.09 (m, 1H), 7.04-6.88 (m, 4H), 3.43 (s, 1H);¹³C NMR (75 MHz, CDCl₃) δ 157.30, 156.15, 132.14, 130.00, 124.04,123.95, 119.88, 119.04; IR(film) 3038 (w), 1583 (s), 1484 (s), 1236 (s),1166 (s) cm⁻¹; m/z (EI) 202 (M⁺, 100%; HRMS (EI) calcd. for C₁₂H₁₀OS202.0452, found 202.0454.

[0185] (D.) 3-(4-Phenoxyphenylsulfanyl)-1-propene (11).

[0186] To a mixture of compound 10 (516 mg, 2.7 mmol) and potassiumcarbonate (534 mg, 3.9 mmol) in DMF (5 mL), allyl bromide (253 μL, 2.9mmol) was added in one portion. The mixture was stirred at roomtemperature overnight. The crude reaction mixture was poured into ether(200 mL), washed with saturated aqueous potassium carbonate (25 mL), andbrine (6×50 mL). The organic layer was dried over magnesium sulfate andconcentrated in vacuo to give a yellow oil. The crude material waspurified by column chromatography ,(silica, 98:2 hexanes:ethyl acetate)to obtain the title compound as a pale yellow oil (598 mg, 93%). ¹H NMR(300 MHz, CDCl₃) δ 7.38-7.32 (m, 4H), 7.15-7.10 (m, 1H), 7.04-7.00 (m,2H), 6.97-6.92 (m, 2H), 5.92-5.82 (m, 1H), 5.10-5.04 (m, 2H), 3.50 (d,J=7.2 Hz, 2H); ¹³C NMR (75 MHz, CDCl₃) δ 157.14, 156.73, 134.01, 133.22,130.05, 129.50, 123.75, 119.40, 119.25, 117.81, 38.84; IR(film) 3078(w), 3039 (w), 1582 (s), 1484 (s), 1240 (s), 1165 (s) cm⁻¹; m/z (EI) 242(M+, 100%), 201 ([M-allyl]⁺, 100); HRMS (EI) calcd. for C₁₅H₁₄OS242.0765, found 242.0764.

Example 2

[0187] 2-(4-Phenoxyphenylsulfonyl)ethyloxirane (5).

[0188] The title compound was prepared in the same manner as describedfor 4, with the exception that compound 12 was used in place of compound11, and the reaction time was 2 days. The title compound was obtained asa white solid (78%). m.p. 75-77° C.; ¹H NMR (500 MHz, CDCl₃) δ 7.84-7.80(m, 2H), 7.44-7.38 (m, 2H), 7.24-7.20 (m, 1H), 7.09-7.04 (m, 4H),3.25-3.15 (m, 2H), 3.02-2.97 (m, 1H), 2.76 (t, J=4.3 Hz, 1H), 2.49 (dd,J=3.0 and 5.0 Hz, 1H), 2.19-2.10 (m, 1H), 1.86 (m, 1H); ³C NMR (125 MHz,CDCl₃) δ 162.93, 155.02, 130.58, 130.81, 125.47, 120.69, 117.91, 53.15,50.32, 47.29, 26.23; IR(KBr disc) 3040 (s), 1580 (s), 1490 (s), 1320(s), 1248 (s), 1148 cm⁻¹; m/z (EI) 304 (M⁺, 80%), 233 (50), 217 (100);HRMS (EI) calcd. for C₁₆H₁₆O₄S 304.0769, found 304.0768.

[0189] (A.) 4-(4-Phenoxyphenylsulfanyl)-1-butene (12).

[0190] The title compound was prepared in the same manner as describedfor 11, with the exception that 4-bromo-1-butene was used in place ofallyl bromide. Compound 12 was obtained as a colorless oil (88%). ¹H NMR(400 MHz, CDCl₃) δ 7.37-7.32 (m, 4H), 7.14-7.10 (m, 1H), 7.04-7.00 (m,2H), 6.96-6.88 (m, 2H), 5.90-5.80 (m, 1H), 5.12-5.02 (m, 2H), 2.98 (m,2H), 2.41-2.34 (m, 2H); ¹³C NMR (100 MHz, CDCl₃) δ 157.18, 156.50,136.65, 132.57, 130.05, 123.72, 119.55, 119.21, 116.47, 34.65, 33.71;IR(film) 3076 (w), 2923 (w), 1583 (s), 1485 (s), 1239 (s) cm⁻¹; m/z (EI)256 (M⁺, 100%), 215 ([M-allyl]⁺, 90), 202 (15); HRMS (EI) calcd. forC₁₆H₁₆OS 256.0922found 256.0922.

Example 3

[0191] 3-(4-Phenoxyphenylsulfonyl)propyloxirane (6).

[0192] The title compound was prepared in the same manner as describedfor 4, with the exception that compound 13 was used in place of compound11, and that the reaction time was 3 days. The title compound wasobtained as a white solid (94%). ¹H NMR (500 MHz, CDCl₃) δ7.86-7.80 (m,2H), 7.44-7.39 (m, 2H), 7.25-7.22 (m, 1H), 7.10-7.04 (m, 4H), 3.21-3.08(m, 2H), 2.90-2.86 (m, 1H), 2.74 (t, J=4.5 Hz, 1H), 2.45 (dd, J=2.5 and4.5 Hz, 1H), 1.92 (quin, J=7.0 Hz, 2H), 1.85-1.78 (m, 1H), (m, 1H); ¹³CNMR (125 MHz, CDCl₃) δ 162.84, 155.08, 130.58, 130.48, 125.43, 120.70,117.88, 56.28, 51.64, 46.86, 31.17, 20.12; IR(KBr disc) 3063 (w), 2923(w), 1582 (s), 1488 (s), 1294 (s), 1246 (s), 1142 (s) cm⁻¹; m/z (EI) 318(M⁺, 40%), 290 (20), 217 (100%); HRMS (EI) calcd. for C₁₇H₁₈O₄S318.0926, found 318.0924.

[0193] (A.) 5-(4-Phenoxyphenylsulfanyl)-1-pentene (13).

[0194] The title compound was prepared in the same manner as describedfor 11, with the exception that 5-bromo-1-pentene was used in place ofallyl bromide. The title compound was obtained as a colorless oil (65%).¹H NMR (500 MHz, CDCl₃) δ 7.37-7.34 (m, 4H), 7.13-7.09 (m, 1H),7.03-7.00 (m, 2H), 6.96-93 (m, 2H), 5.83-5.74 (m, 1H), 5.06-4.98 (m,2H), 2.88 (t, J=7.0 Hz, 2H), 2.22-2.16 (m, 2H), 1.73 (q, J=7.0 Hz, 2H);¹³C NMR (125 MHz, CDCl₃) δ 157.23, 156.36, 137.84, 132.30, 130.41,130.03, 123.67, 11 9.55, 119.16, 115.62, 34.61, 32.86, 28.6 1; IR(film)3075 (w), 2929 (m), 1583 (s), 1484 (s), 1236 (s) cm⁻¹; m/z (EI) 270 (M⁺,100%), 215 (70), 202 (60); HRMS (EI) calcd. for C₁₇H₁₈OS 270.1078, found270.1076.

Example 4

[0195] (4-Phenoxyphenylsulfonyl)methylthiirane (1).

[0196] To a solution of compound 4 (710 mg, 2.5 mmol) in THF (5 mL), asolution of ammonium thiocyanate (559 mg, 7.4 mmol) in water (3 mL) wasadded. The reaction was stirred at room temperature for 16 hours, afterwhich time it was poured into ethyl acetate (100 mL), and then washedwith water (25 mL), followed by brine (25 mL). The organic phase wasdried over magnesium sulfate and was concentrated to give a white oil.The crude material was purified by column chromatography (silica, 8:1hexanes:ethyl acetate) to obtain compound 1 as a white solid (102 mg,14%). m.p. 99-101° C.; ¹H NMR (500 MHz, CDCl₃) δ 7.89-7.84 (m, 2H),7.46-7.40 (m, 2H), 7.26-7.22 (m, 1H), 7.11-6.96 (m, 4H), 3.52 (dd, J=5.5and 14.5 Hz, 1H), 3.17 (dd, J=7.5 and 14.5 Hz, 1H), 3.09-3.03 (m, 1H),2.53 (dd, J=2.0 and 6.0 Hz, 1H) 2.16 (dd, J=2.0 and 5.0 Hz, 1H); ¹³C NMR(125 MHz, CDCl₃) δ 163.20, 155.02, 132.13, 130.95, 130.52, 125.52,120.69, 117.97, 62.90, 26.31, 24.47; IR(KBr disc) 3030 (w), 1583 (s),1486 (s), 1317 (s), 1246 (s), 1141 (s) cm⁻¹; m/z (EI) 306 (M⁺, 2%), 242([M-SO₂]⁺, 35); HRMS (EI) calcd. for C₁₅H₁₄O₃S₂ 306.0384, found306.0382.

Example 5

[0197] 2-(4-Phenoxyphenylsulfonyl)ethylthiirane (2).

[0198] The title compound was prepared in the same manner as describedfor 1, with the exception that compound 5 was used in place of compound4. The crude material was purified by column chromatography (silica, 2:1hexanes:ethyl acetate) to give the title compound as a white solid(93%). m.p. 99-101° C.; ¹H NMR (500 MHz, CDCl₃) 8 7.83 (d, J=8.0 Hz,2H), 7.42 (t, J=8.0 Hz, 2H), 7.26-7.22 (m, 1H), 7.10-7.06 (m, 4H),3.30-3-20 (m, 2H), 2.98-2.92 (m, 1H), 2.52 (dd, J=1 and 6 Hz, 1H),2.48-2.39 (m, 1H), 2.18 (dd, J=1 and 5 Hz, 1H), 1.78-1.69 (m, 1H); ¹³CNMR (125 MHz, CDCl₃) δ 162.94, 155.03, 132.50, 130.55, 130.51, 125.48,120.71, 117.92, 55.97, 33.62, 29.82, 26.05; IR(KBr disc) 3040 (w), 1583(s), 1487 (s), 1256 (s), 1142 (s) cm⁻¹; m/z (EI) 320 (M⁺, 50%),288,(20), 234 (40), 217 (60), 170 (100); HRMS (EI) calcd. for C₁₆H₁₆O₃S₂320.0541, found 320.0540.

Example 6

[0199] 3-(4-Phenoxyphenylsulfonyl)propylthiirane (3).

[0200] The title compound was prepared in the same manner as describedfor 1, with the exception that compound 6 was used in place of compound4. The crude material was purified by column chromatography (silica, 2:1hexanes:ethyl acetate) to give the title compound as a white solid(85%). m.p. 75-76° C.; ¹H NMR (500 MHz, CDCl₃) δ 7.85-7.82 (m, 2H),7.44-7.40 (m, 2H), 7.26-7.22 (m, 1H), 7.10-7.06 (m, 4H), 3.20-3.09 (m,2H), 2.84-2.79 (m, 1H), 2.50 (dd, J=1 and 6 Hz, 1H), 2.14 (dd, J=1 and5.5 Hz, 1H), 2.12-2.06 (m, 1H), 1.97 (quin, J=8 Hz, 2H), 1.45-1.38 (m,1H); ¹³C NMR (125 MHz, CDCl₃) δ 162.85, 155.08, 132.55, 130.60, 130.49,125.43, 120.69, 117.91, 56.09, 35.13, 34.86, 25.72, 22.92; IR(KBr disc)3000 (w), 1583 (s), 1480 (s), 1254 (s), 1143 (s) cm⁻¹; m/z (EI) 334 (M⁺,30%), 301 (10), 234 (100), 217 (70), 170 (70); HRMS (EI) calcd. forC₁₇H₁₈O₃S₂ 334.0697, found 334.06.

Example 7

[0201] TABLE 1 Kinetics parameters for inhibition of MMPs by compoundsof the present invention k_(on)(M⁻¹s⁻¹) × 10 ⁻⁴ k_(off)(s⁻¹) × 10³K_(i)(μM) Compound 1 MMP-2 11 ± 1  1.5 ± 0.6a 0.0139 ± 0.0004 1.8 ± 0.1MMP-9 1.4 ± 0.3  9 ± 1^(a) 0.6 ± 0.2 7.1 ± 0.5 MMP-3 (1.8 ± 0.4) ± 10⁻² 2.7 ± 0.9^(a) 15 ± 6  5.5 ± 0.4 MMP-7 96 ± 41 Compound 2 MMP-2 4.7 ±0.7 MMP-9 44 ± 5  MMP-3 NI^(b) MMP-7 NI MMP-1 NI Compound 3 MMP-2 4.3 ±0.7 MMP-9 181 ± 41  MMP-3 NI MMP-7 NI MMP-1 NI Compound 4 MMP-2 25 ± 2 MMP-9 186 ± 11  MMP-3 NI MMP-7 NI MMP-1 NI TIMP-1^(c) MMP-2 4.4 ± 0.11.3 ± 0.2 0.029 ± 0.005 MMP-9 5.2 ± 0.1 1.2 ± 0.2 0.024 ± 0.004TIMP-2^(c) MMP-2 3.3 ± 0.1 0.8 ± 0.1 0.023 ± 0.004 MMP-9 2.2 ± 0.1 1.3 ±0.2 0.058 ± 0.007 Compound 5 MMP-2 5.1 ± 0.5 MMP-9 102 ± 2  MMP-3 NI^(a)MMP-7 NI MMP-1 NI Compound 6 MMP-2 10.7 ± 0.6 MMP-9 75 ± 6 MMP-3 NI^(b)MMP-7 NI MMP-1 NI

[0202] All publications, patents, and patent documents are incorporatedby reference herein, as though individually incorporated by reference.The invention has been described with reference to various specific andpreferred embodiments and techniques. However, it should be understoodthat many variations and modifications may be made while remainingwithin the spirit and scope of the invention. In addition, somereferences were obtained on the world wide web (www). These referencesare also incorporated by reference herein, as though individuallyincorporated by reference.

What is claimed is:
 1. A compound of formula (I):

wherein A—X—M is a hydrophobic group; D is O, S, (C₁-C₆)alkyl, a directbond, SO₂, SO, C(═O)NR, C(═O)O, NRC(═O), or OC(═O); E is a direct bond,(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl, (C₂-C₆)alkenyl, or (C₂-C₆)alkynyl,wherein any alkyl, cycloalkyl, alkenyl, or alkynyl of E is optionallysubstituted with one or more (C₁-C₆)alkyl, hydroxy, (C₁-C₆)alkoxy,cyano, nitro, halo, SR, NRR, or COOR, wherein each R is independently Hor (C₁-C₆)alkyl; J is S or O; G, T, and Q are each independently H,(C₁-C₆)alkyl, or cyano; or a pharmaceutically acceptable salt thereof.2. The compound of claim 1 wherein A—X—M is a saturated or partiallyunsaturated hydrocarbon chain comprising one or more carbon atoms andoptionally comprising one or more oxy (—O—), thio (—S—), sulfinyl(—SO—), sulfonyl (S(O)₂—), or NRf in the chain, wherein each Rf isindependently hydrogen or (C₁-C₆)alkyl; wherein the saturated orpartially unsaturated hydrocarbon chain is optionally substituted withone or more oxo (═O), hydroxy, cyano, halo, nitro, trifluoromethyl,trifluoromethoxy, (C₁-C₆)alkyl, (C₁-C₆)alkoxy,(C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl, aryl, heteroaryl,(C₃-C₈)cycloalkyl(C₁-C₆)alkyl, (aryl)(C,-C₈)alkyl,(heteroaryl)(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl oxy, (aryl)oxy,(heteroaryl)oxy, (C₃-C₈)cycloalkyl, (aryl)oxy(aryl),(heteroaryl)oxy(heteroaryl), (C₃-C₈)cycloalkyl oxy (C₁-C₆)alkyl,(aryl)oxy (C₁-C₆)alkyl, or (heteroaryl)oxy (C₁-C₆)alkyl; and wherein anyaryl, (C₃-C₈)cycloalkyl, or heteroaryl is optionally substituted withone or more oxo (═O), hydroxy, cyano, halo, nitro, trifluoromethyl,trifluoromethoxy, (C₁-C₆)alkyl, (C₁-C₆)alkoxy,(C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl, aryl, heteroaryl,(C₃-C₈)cycloalkyl(C₁-C₆)alkyl, (aryl)(C₁-C₈)alkyl,(heteroaryl)(C₁-C₆)alkyl, (C₃-C₈)cycloalkyl oxy, (aryl)oxy,(heteroaryl)oxy, (C₃-C₈)cycloalkyl, (aryl)oxy(aryl),(heteroaryl)oxy(heteroaryl), (C₃-C₈)cycloalkyl oxy (C₁-C₆)alkyl,(aryl)oxy (C₁-C₆)alkyl, or (heteroaryl)oxy (C₁-C₆)alkyl.
 3. The compoundof claim 1 wherein A and M are each independently phenyl or monocyclicheteroaryl, wherein any phenyl or monocyclic heteroaryl is optionallysubstituted with one or more hydroxy, (C₁-C₆)alkyl, (C₁-C₆)alkanoyl,(C₁-C₆)alkanoyloxy, (C₁-C₆)alkoxy, cyano, nitro, halo, trifluoromethyl,trifluoromethoxy, SR, NRR, or COOR; and X is O, S, SO, SO₂, C(═O)NR,C(═O)O, NRC(═O), OC(═O), NR, a direct bond, or (C₁-C₆)alkyl optionallysubstituted with one or more hydroxy, (C₁-C₆)alkoxy, cyano, nitro, halo,SR, NRR, or COOR.
 4. The compound of claim 1 wherein A-X-M is bicyclicaryl, bicyclic heteroaryl, or bicyclic alkyl; wherein any aryl,heteroaryl or alkyl is optionally substituted with one or more hydroxy,(C₁-C₆)alkyl, (C₁-C₆)alkanoyl, (C₁-C₆)alkanoyloxy, (C₁-C₆)alkoxy, cyano,nitro, halo, trifluoromethyl, trifluoromethoxy, SR, NRR, or COOR;wherein each R is independently H, (C₁-C₆)alkyl, phenyl, benzyl, orphenethyl.
 5. The compound of claim 1 wherein A—X—M is bicyclic aryl,bicyclic heteroaryl, or bicyclic alkyl.
 6. The compound of claim 1wherein A—X—M is:

wherein X′ is O, CH₂, or a direct bond; Y′ is N or CH₂; and Z′ is halo,OCH₃, or hydroxy.
 7. The compound of claim 1 wherein A—X—M is:

wherein each W′ is independently N or CH; and Z′ is halo, OCH₃, orhydroxy.
 8. The compound of claim 1 wherein A—X—M is:

wherein n′ is about 1 to about 4; and Z′ is halo, OCH₃, or hydroxy. 9.The compound of claim 1 wherein A—X—M is:

wherein R′ is O, CH₂, or S; and m′ is about 2 to about
 7. 10. Thecompound of claim 1 wherein A—X—M is:

wherein n′ is about 1 to about
 4. 11. The compound of claim 1 whereinA—X—M is:

wherein R′ is O, CH₂, or S.
 12. The compound of claim 1 wherein A—X—M isnaphthyl.
 13. The compound of claim 1 wherein A is phenyl.
 14. Thecompound of claim 1 wherein M is phenyl.
 15. The compound of claim 1wherein X is O.
 16. The compound of claim 1 wherein D is SO₂.
 17. Thecompound of claim 1 wherein E is (C₁-C₆)alkyl.
 18. The compound of claim1 wherein E is methyl.
 19. The compound of claim 1 wherein J is S. 20.The compound of claim 1 wherein G is hydrogen.
 21. The compound of claim1 wherein T is hydrogen.
 22. The compound of claim 1 wherein Q ishydrogen.
 23. The compound of claim 1 wherein A is phenyl, M is phenyl,X is O, D is SO₂, E is methyl, J is S, G is hydrogen, T is hydrogen, andQ is hydrogen.
 24. A pharmaceutical composition comprising a compound ofclaim 1; and a pharmaceutically acceptable carrier.
 25. A radiolabeledcompound comprising a compound of formula (I) as described in claim 1,and a radionuclide.
 26. The compound of claim 25 wherein theradionuclide is a non-metallic radionuclide.
 27. The compound of claim26 wherein the non-metallic radionuclide is Fluorine-19, Carbon-11,Fluorine-18, Iodine-123, or Bromine-76.
 28. The compound of claim 25wherein the compound comprises a chelating group comprising a detectableradionuclide.
 29. The compound of claim 28 wherein the detectableradionuclide is a metallic radionuclide.
 30. The compound of claim 29wherein the metallic radionuclide is Antimony-124, Antimony-125,Arsenic-74, Barium-103, Barium-140, Beryllium-7, Bismuth-206,Bismuth-207, Cadmium-109, Cadmium-115m, Calcium-45, Cerium-139,Cerium-141, Cerium-144, Cesium-137, Chromium-51, Cobalt-55, Cobalt-56,Cobalt-57, Cobalt-58, Cobalt-60, Cobalt-64, Copper-67, Erbium-169,Europium-152, Gallium-64, Gallium-68, Gadolinium-153, Gadolinium-157Gold-195, Gold-199, Hafnium-175, Hafnium-175-181, Holmium-166,Indium-110, Indium-111, Iridium-192, Iron-55, Iron-59, Krypton-85,Lead-210, Manganese-54, Mercury-197, Mercury-203, Molybdenum-99,Neodymium-147, Neptunium-237, Nickel-63, Niobium-95, Osmium-185+191,Palladium-103, Platinum-195m, Praseodymium-143, Promethium-147,Protactinium-233, Radium-226, Rhenium-186, Rhenium-188, Rubidium-86,Ruthenium-103, Ruthenium-106, Scandium-44, Scandium-46, Selenium-75,Silver-110m, Silver-111, Sodium-22, Strontium-85, Strontium-89,Strontium-90, Sulfur-35, Tantalum-182, Technetium-99m, Tellurium-125,Tellurium-132, Thallium-204, Thorium-228, Thorium-232, Thallium-170,Tin-113, Tin-114, Tin-117m, Titanium-44, Tungsten-185, Vanadium-48,Vanadium-49, Ytterbium-169, Yttrium-86, Yttrium-88, Yttrium-90,Yttrium-91, Zinc-65, or Zirconium-95.
 31. A pharmaceutical compositioncomprising a compound of claim 25; and a pharmaceutically acceptablecarrier.
 32. A method for treating or preventing cancer, angiogenesis,arthritis, connective tissue disease, cardiovascular disease,inflammation or autoimmune disease in a mammal inflicted with or at riskthereof comprising administering to the mammal in need of such treatmentor prevention an effective amount of a compound of claim
 1. 33. Themethod of claim 32 further comprising administering a chemotherapeuticagent, or a pharmaceutically acceptable salt thereof.
 34. A method forinhibiting a matrix metalloproteinase comprising a zinc atom, the methodcomprising contacting the matrix metalloproteinase with a compound witha group that can be activated for nucleophilic substitution by the zincatom and can form a covalent bond with a nucleophile of the matrixmetalloproteinase.
 35. The method of claim 34 wherein the matrixmetalloproteinase is a gelatinase, collagenase, stromelysin,membrane-type MMP, or matrilysin.
 36. The method of claim 34 wherein thecontacting is in vitro.
 37. The method of claim 34 wherein thecontacting is in vivo.
 38. The method of claim 34 wherein the compoundis a compound as described in claim
 1. 39. The method of claim 34wherein the group is a thiirane ring.
 40. The method of claim 34 whereinthe compound comprises a second group that can form one or more hydrogenbonds with an electrophile of the matrix metalloproteinase.
 41. Themethod of claim 40 wherein the second group is SO₂.
 42. A method forinhibiting a gelatinase comprising a zinc atom, the method comprisingcontacting the gelatinase with a compound with a group that can beactivated for nucleophilic substitution by the zinc atom and can form acovalent bond with a nucleophilic site of the gelatinase.
 43. The methodof claim 42 wherein the contacting is in vitro.
 44. The method of claim42 wherein the contacting is in vivo.
 45. The method of claim 42 whereinthe compound is a compound of claim
 1. 46. The method of claim 42wherein the group is a thiirane.
 47. The method of claim 42 wherein thecompound comprises a second group that can form one or more hydrogenbonds with an electrophile of the gelatinase.
 48. The method of claim 47wherein the second group is SO₂.
 49. The method of claim 42 wherein thegelatinase is MMP-2 or MMP-9.
 50. A method for imaging a tumor in amammal inflicted with a tumor comprising administering to the mammal aneffective amount of a compound of claim 25, or a pharmaceuticallyacceptable salt thereof, and detecting the presence of the compound. 51.The method of claim 50 wherein the mammal is a human.
 52. A method forpreventing ovulation in a mammal at risk thereof comprisingadministering to the mammal an effective amount of a compound ofclaim
 1. 53. A method for preventing the implantation of a fertilizedegg into the uterus of a mammal in need thereof comprising administeringto the mammal an effective amount of a compound of claim 1.